76066-07-4

Basic information

• Product Name: 2-Bromo-3-methoxy-6-nitropyridine
• Synonyms: 2-Bromo-3-methoxy-6-nitropyridine;Pyridine, 2-bromo-3-methoxy-6-nitro-;6-Bromo-5-methoxy-2-nitropyridine
• CAS NO: 76066-07-4
• Molecular Formula: C₆H₅BrN₂O₃
• Molecular Weight: 233.02
• EINECS: 675-760-5
• Product Categories: blocks;Bromides;NitroCompounds;Pyridines;Heterocyclic Compounds;Heterocycles
• Mol File: 76066-07-4.mol
• Article Data: 17

Chemical Properties

• Melting Point: 140-1420C
• Boiling Point: 364.404 °C at 760 mmHg
• Flash Point: 174.185 °C
• Appearance: /
• Density: 1.73g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.587
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: -10.90±0.10(Predicted)
• CAS DataBase Reference: 2-Bromo-3-methoxy-6-nitropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-3-methoxy-6-nitropyridine(76066-07-4)
• EPA Substance Registry System: 2-Bromo-3-methoxy-6-nitropyridine(76066-07-4)

Safety Data

• Hazardous Substances Data: 76066-07-4(Hazardous Substances Data)

Usage

Chemical Properties

Off-White Solid

InChI:InChI=1/C6H5BrN2O3/c1-12-4-2-3-5(9(10)11)8-6(4)7/h2-3H,1H3

Synthetic route

2-bromo-3-methoxypyridine (24100-18-3) → 2-bromo-3-methoxy-6-nitropyridine (76066-07-4)

Conditions	Yield
With sulfuric acid; nitric acid at 2 - 55℃;	83%
With sulfuric acid; nitric acid at 60℃; for 1h;	80%
With sulfuric acid; nitric acid at 50℃; for 4h;	80%

3-HYDROXYPYRIDINE (109-00-2) → 2-bromo-3-methoxy-6-nitropyridine (76066-07-4)

Conditions	Yield
Multi-step reaction with 3 steps 1: 35 percent / Br2, 10percent aq. NaOH / 24 h 2: 1.) NaOCH3 / 1.) MeOH, DMF; 2.) DMF, RT, 1.5 h 3: 80 percent / fuming HNO3, conc. H2SO4 / 1 h / 60 °C View Scheme

2-bromo-pyridin-3-ol (6602-32-0) → 2-bromo-3-methoxy-6-nitropyridine (76066-07-4)

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.) NaOCH3 / 1.) MeOH, DMF; 2.) DMF, RT, 1.5 h 2: 80 percent / fuming HNO3, conc. H2SO4 / 1 h / 60 °C View Scheme

2-bromo-3-methoxypyridine (24100-18-3) + sulfuric acid (7664-93-9) → 2-bromo-3-methoxy-6-nitropyridine (76066-07-4)

Conditions	Yield
With nitric acid In water

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2-amino-5-methoxypyridine (10167-97-2)

Conditions	Yield
With hydrazine; palladium 10% on activated carbon In ethanol for 0.75h; Heating / reflux;	96%
With hydrazine; palladium 10% on activated carbon In ethanol; water for 0.75h; Heating / reflux;	96%
With hydrazine hydrate; palladium on activated charcoal In ethanol for 1.5h; Heating;	95%

methanol (67-56-1) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2,3-dimethoxy-6-nitropyridine (79491-44-4)

Conditions	Yield
With sodium In dimethyl sulfoxide at 30℃; for 2h;	81%

zinc(II) cyanide (557-21-1) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-methoxy-6-nitropicolinonitrile

Conditions	Yield
In N,N-dimethyl-formamide at 120℃; for 4h;	78%

sodium methylate (124-41-4) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2,3-dimethoxy-6-nitropyridine (79491-44-4)

Conditions	Yield
In methanol; dimethyl sulfoxide at 20 - 35℃; for 49.5h;	76%

methanol (67-56-1) + sodium methylate (124-41-4) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2,3-dimethoxy-6-nitropyridine (79491-44-4)

Conditions	Yield
In dimethyl sulfoxide at 20 - 35℃; for 49.5h;	76%

2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (72824-04-5) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2-allyl-3-methoxy-6-nitropyridine (1446792-80-8)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 66℃; for 20h;	75%
With tetrakis(triphenylphosphine) palladium(0); cesium fluoride In tetrahydrofuran at 66℃; for 20h;	75%
With tetrakis(triphenylphosphine) palladium(0); cesium fluoride In tetrahydrofuran at 66℃; for 20h;	75%

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) + 2-isopropenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (126726-62-3) → 3-methoxy-6-nitro-2-(prop-1-en-2-yl)pyridine (1446792-90-0)

Conditions	Yield
With potassium phosphate; tetrakis(triphenylphosphine) palladium(0) In water; dimethyl amine at 150℃; for 0.333333h; Microwave irradiation; Sealed tube;	66%
With tetrakis(triphenylphosphine) palladium(0); cesium fluoride In aq. phosphate buffer; N,N-dimethyl acetamide; water at 150℃; for 0.333333h;	66%
With potassium phosphate; tetrakis(triphenylphosphine) palladium(0) In N,N-dimethyl acetamide; water at 150℃; for 0.333333h; Microwave irradiation; Sealed tube;	66%

sodium hydrosulfite (Na2 Ss O4) + 2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 6-bromo-5-methoxypyridin-2-amine (79491-43-3)

Conditions	Yield
With ammonium hydroxide In dichloromethane; water	50%

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 6-bromo-5-methoxypyridin-2-amine (79491-43-3)

Conditions	Yield
With hydrogen; platinum(IV) oxide In ethanol under 760 Torr;	46%

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 2-bromo-5-methoxypyridine (105170-27-2)

Conditions	Yield
Multi-step reaction with 2 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 5-methoxy-2-pyridinecarboxaldehyde (22187-96-8)

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: aq. HCl View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-(5-Methoxypyridin-2-ylmethyl)-1-methyl-2,3-dihydro-1H-indol (325796-80-3)

Conditions

Yield

Multi-step reaction with 5 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 40 percent / tetrahydrofuran; hexane / -100 °C 4.1: 85 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 1.5 h / 20 °C / 52504.2 Torr 5.1: 71 percent / NaBH3CN; TFA / acetic acid View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-(5-Methoxypyridin-2-ylmethyl)-2,3-dihydroindol-1-carbonsaeuremethylester (325796-82-5)

Conditions	Yield
Multi-step reaction with 6 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: NaBH3CN / methanol; acetic acid / 3.5 h 4.2: 82 percent / NaBH3CN; TFA / 16.5 h 5.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr 6.1: 94 percent / aq. NaHCO3 / diethyl ether / 0 °C View Scheme
Multi-step reaction with 7 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr 5.1: 86 percent / TFA; NaBH3CN / acetic acid 6.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr 7.1: 94 percent / aq. NaHCO3 / diethyl ether / 0 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 5-Methoxy-2-(1-methoxycarbonyl-2,3-dihydro-1H-indol-3-ylmethyl)-1-methylpyridiniumiodid

Conditions	Yield
Multi-step reaction with 7 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: NaBH3CN / methanol; acetic acid / 3.5 h 4.2: 82 percent / NaBH3CN; TFA / 16.5 h 5.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr 6.1: 94 percent / aq. NaHCO3 / diethyl ether / 0 °C 7.1: 92 percent / acetone / 120 h View Scheme
Multi-step reaction with 8 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr 5.1: 86 percent / TFA; NaBH3CN / acetic acid 6.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr 7.1: 94 percent / aq. NaHCO3 / diethyl ether / 0 °C 8.1: 92 percent / acetone / 120 h View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1‐(5‐methoxypyridin‐2‐yl)ethan‐1‐one (325796-84-7)

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: tetrahydrofuran; hexane / -100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-(5-Methoxypyridin-2-ylmethyl)-2,3-dihydro-1H-indol (325796-81-4)

Conditions	Yield
Multi-step reaction with 5 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: NaBH3CN / methanol; acetic acid / 3.5 h 4.2: 82 percent / NaBH3CN; TFA / 16.5 h 5.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr View Scheme
Multi-step reaction with 6 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr 5.1: 86 percent / TFA; NaBH3CN / acetic acid 6.1: 95 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 45003.6 Torr View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-(5-Methoxypyridin-2-ylmethyl)-1H-indol

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 10 percent / tetrahydrofuran; hexane / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-(1H-Indol-3-yl)-1-(5-methoxypyridin-2-yl)-methanol (325796-74-5)

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 10 percent / tetrahydrofuran; hexane / -100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-(1-Methoxymethyl-1H-indol-3-yl)-1-(5-methoxypyridin-2-yl)-methanol (325796-73-4)

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 40 percent / tetrahydrofuran; hexane / -100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-Methoxymethyl-3-(5-methoxypyridin-2-ylmethyl)-1H-indol (325796-77-8)

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 40 percent / tetrahydrofuran; hexane / -100 °C 4.1: 85 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 1.5 h / 20 °C / 52504.2 Torr View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 3-[1-Hydroxy-1-(5-methoxypyridin-2-yl)-methyl]-indol-1-carbonsaeuremethylester

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / -105 - -100 °C 3.2: 34 percent / tetrahydrofuran; hexane / -100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-Benzyl-3-(5-methoxypyridin-2-ylmethyl)-1H-indol (325796-76-7)

Conditions

Yield

Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-Benzyl-3-(5-methoxypyridin-2-ylmethyl)-2,3-dihydro-1H-indol (325796-79-0)

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: NaBH3CN / methanol; acetic acid / 3.5 h 4.2: 82 percent / NaBH3CN; TFA / 16.5 h View Scheme
Multi-step reaction with 5 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: 100 percent / H2 / 5 percent Pd/C / ethanol; aq. HCl / 3 h / 20 °C / 52504.2 Torr 5.1: 86 percent / TFA; NaBH3CN / acetic acid View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 1-(1-Benzyl-1H-indol-3-yl)-1-(5-methoxypyridin-2-yl)-methanol (325796-72-3)

Conditions	Yield
Multi-step reaction with 3 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → C23H24BN3O

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: NaBH3CN / methanol; acetic acid / 3.5 h 4.2: NaBH3CN; TFA / 16.5 h View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → Bis-(1-benzylindol-3-yl)-5-methoxypyridin-2-yl-methan

Conditions	Yield
Multi-step reaction with 4 steps 1.1: 95 percent / N2H4*H2O / 5 percent Pd/C / ethanol / 1.5 h / Heating 2.1: Br2 / aq. HBr / cooling 2.2: 67 percent / aq. NaNO2 / 0.5 h / cooling 3.1: BuLi / tetrahydrofuran; hexane / 0.33 h / -105 - -100 °C 3.2: 60 percent / tetrahydrofuran; hexane / 1.5 h / -100 °C 4.1: aq. HCl View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → 5'-Hydroxypiroxicam (77459-78-0)

Conditions	Yield
Multi-step reaction with 3 steps 1: 59 percent / H2, NaOH / 10percent Pd/C / ethanol 2: 59 percent / xylene / 24 h / Heating 3: 30percent HBr, AcOH / 120 h / 100 °C View Scheme

2-bromo-3-methoxy-6-nitropyridine (76066-07-4) → N-(5'-methoxy-2'-pyridyl)-4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide (76066-12-1)

Conditions	Yield
Multi-step reaction with 2 steps 1: 59 percent / H2, NaOH / 10percent Pd/C / ethanol 2: 59 percent / xylene / 24 h / Heating View Scheme

Upstream product

• 24100-18-3 2-bromo-3-methoxypyridine 
• 109-00-2 3-HYDROXYPYRIDINE 
• 6602-32-0 2-bromo-pyridin-3-ol 
• 7664-93-9 sulfuric acid 

Downstream Products

• 79491-44-4 2,3-Dimethoxy-6-nitropyridin 
• 10167-97-2 2-amino-5-methoxypyridine 
• 79491-43-3 6-bromo-5-methoxypyridin-2-amine 
• 105170-27-2 2-bromo-5-methoxypyridine 
• 22187-96-8 5-methoxy-2-pyridinecarboxaldehyde 
• 325796-84-7 1‐(5‐methoxypyridin‐2‐yl)ethan‐1‐one 
• 325796-76-7 1-Benzyl-3-(5-methoxypyridin-2-ylmethyl)-1H-indol 
• 325796-79-0 1-Benzyl-3-(5-methoxypyridin-2-ylmethyl)-2,3-dihydro-1H-indol 
• 325796-72-3 1-(1-Benzyl-1H-indol-3-yl)-1-(5-methoxypyridin-2-yl)-methanol 
• 1446792-88-6 tert-butyl (1S,2R)-2-(6-carbamoyl-5-(5-methoxy-6-propylpyridin-2-ylamino)pyridazin-3-ylamino)cyclohexylcarbamate 
• 1446790-95-9 6-((1R,2S)-2-aminocyclohexylamino)-4-(5-methoxy-6-propylpyridin-2-ylamino)pyridazine-3-carboxamide 
• 955376-51-9 6-methoxyimidazo[1,2-a]pyridine 
• 1100750-16-0 5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-6-ol 

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