anagrelide
Conditions | Yield |
---|---|
With water In ethanol at 23℃; for 3h; | 99% |
anagrelide
Conditions | Yield |
---|---|
Stage #1: ethyl (2‑amino‑5,6‑dichloroquinazoline‑3(4H)‑yl)acetate With sodium hydrogencarbonate In ethanol at 20℃; for 1h; pH=8 - 9; Stage #2: With sodium hydroxide In ethanol at 4 - 20℃; for 1.5h; pH=10 - 11; | 80% |
N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester
chloroformamidine hydrochloride
anagrelide
Conditions | Yield |
---|---|
Stage #1: N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester; chloroformamidine hydrochloride With acetic acid In acetonitrile at 90℃; for 5h; Inert atmosphere; Stage #2: With N-ethyl-N,N-diisopropylamine In acetonitrile for 1.25h; Concentration; Temperature; Time; Solvent; | 73% |
anagrelide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water at 37℃; for 1h; pH=8 - 10; Product distribution / selectivity; |
anagrelide
Conditions | Yield |
---|---|
In water at 37℃; for 1h; pH=7; Product distribution / selectivity; | |
With sodium hydrogencarbonate In water at 37℃; for 1h; pH=8 - 10; Product distribution / selectivity; | |
With sodium hydroxide In water at 37℃; for 1h; Product distribution / selectivity; |
anagrelide
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water at 37℃; for 1h; pH=8 - 10; Product distribution / selectivity; |
ethyl-(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetate
anagrelide
Conditions | Yield |
---|---|
With hydrogenchloride; potassium carbonate In ethylene glycol | |
With acetic acid | 0.116 g (91%) |
With hydrogenchloride In N-methyl-acetamide | 0.070 g (54.7%) |
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetonitrile
anagrelide
Conditions | Yield |
---|---|
With potassium carbonate In ethylene glycol |
anagrelide
Conditions | Yield |
---|---|
With triethylamine In ethanol | 179 g (92%) |
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile
B
anagrelide
Conditions | Yield |
---|---|
With potassium carbonate In ethylene glycol |
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile
B
anagrelide
Conditions | Yield |
---|---|
With potassium carbonate In ethylene glycol |
ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetate
anagrelide
Conditions | Yield |
---|---|
With acetic acid | 0.116 g (91%) |
ethyl-(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetate
B
anagrelide
Conditions | Yield |
---|---|
With hydrogenchloride; potassium carbonate In ethylene glycol |
ethyl-5,6-dichloro-3,4-dihydro-2-(1H)-iminoquinazoline-3-acetate hydrobromide
anagrelide
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol for 2h; Heating / reflux; |
anagrelide
Conditions | Yield |
---|---|
With triethylamine In ethanol at 30℃; for 4h; Reflux; |
4,5-Dichloro-1H-indole-2,3-dione
anagrelide
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 2: hydrogenchloride; borane / tetrahydrofuran 3: hydrogenchloride; thionyl chloride; triethylamine / benzene 4: toluene 5: triethylamine / ethanol View Scheme |
6-amino-2,3-dichlorobenzoic acid
anagrelide
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: hydrogenchloride; borane / tetrahydrofuran 2: hydrogenchloride; thionyl chloride; triethylamine / benzene 3: toluene 4: triethylamine / ethanol View Scheme |
3,4-dichloro-2-hydroxymethylaniline
anagrelide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: hydrogenchloride; thionyl chloride; triethylamine / benzene 2: toluene 3: triethylamine / ethanol View Scheme |
N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester
anagrelide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: toluene 2: triethylamine / ethanol View Scheme |
Conditions | Yield |
---|---|
In water at 60℃; for 3h; | 90% |
Conditions | Yield |
---|---|
With phosphoric acid at 85℃; for 18h; | 77.5% |
anagrelide
anagrelide hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In methanol for 0.166667h; Heating / reflux; | 70% |
With hydrogenchloride In dimethyl sulfoxide at 50℃; | 44.2% |
With hydrogenchloride In ethanol; water at 78 - 80℃; for 0.133333h; |
anagrelide
Conditions | Yield |
---|---|
With hydrogenchloride; water In ethanol at 20℃; for 2h; Time; Solvent; |
The Imidazo[2,1-β]quinazolin-2(3H)-one,6,7-dichloro-1,5-dihydro-, with the CAS registry number 68475-42-3, is also known as Anagrelide. It belongs to the product category of Drugs. This chemical's molecular formula is C10H7Cl2N3O and molecular weight is 256.09. What's more, its systematic name is 6,7-Dichloro-5,10-dihydroimidazo[2,1-β]quinazolin-2(3H)-one and its IUPAC name is 6,7-Dichloro-5,10-dihydro-3H-imidazo[2,1-β]quinazolin-2-one.
Physical properties about Imidazo[2,1-β]quinazolin-2(3H)-one,6,7-dichloro-1,5-dihydro- are: (1) ACD/LogP: 1.96; (2) # of Rule of 5 Violations: 0; (3) ACD/LogD (pH 5.5): 1.96; (4) ACD/LogD (pH 7.4): 1.96; (5) ACD/BCF (pH 5.5): 18.19; (6) ACD/BCF (pH 7.4): 18.19; (7) ACD/KOC (pH 5.5): 277.51; (8) ACD/KOC (pH 7.4): 277.62; (9) #H bond acceptors: 4; (10) #H bond donors: 1; (11) #Freely Rotating Bonds: 0; (12) Polar Surface Area: 35.91 Å2; (13) Index of Refraction: 1.79; (14) Molar Refractivity: 61.09 cm3; (15) Molar Volume: 144.1 cm3; (16) Polarizability: 24.22×10-24cm3; (17) Surface Tension: 67.3 dyne/cm; (18) Density: 1.77 g/cm3; (19) Flash Point: 181.5 °C; (20) Enthalpy of Vaporization: 62.42 kJ/mol; (21) Boiling Point: 376.5 °C at 760 mmHg; (22) Vapour Pressure: 7.21E-06 mmHg at 25 °C; (23) Melting point: 280 °C.
Preparation of Imidazo[2,1-β]quinazolin-2(3H)-one,6,7-dichloro-1,5-dihydro-: this chemical is prepared by reaction of Ethyl (2-cyanoimino-5,6-dichlorine-1,2,3,4-tetrahydroquinazolin-3-yl)acetate with Acetic acid.
The reaction time is 0.5 hour and the temperature is 100 °C. The yield is 91%.
You can still convert the following datas into molecular structure:
(1) SMILES: C1C2=C(C=CC(=C2Cl)Cl)NC3=NC(=O)CN31
(2) InChI: InChI=1S/C10H7Cl2N3O/c11-6-1-2-7-5(9(6)12)3-15-4-8(16)14-10(15)13-7/h1-2H,3-4H2,(H,13,14,16)
(3) InChIKey: OTBXOEAOVRKTNQ-UHFFFAOYSA-N
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