Product Name

  • Name

    Anagrelide

  • EINECS 1312995-182-4
  • CAS No. 68475-42-3
  • Article Data14
  • CAS DataBase
  • Density 1.77 g/cm3
  • Solubility slightly soluble in water
  • Melting Point 280 °C
  • Formula C10H7Cl2N3O
  • Boiling Point 376.5 °C at 760 mmHg
  • Molecular Weight 256.091
  • Flash Point 181.5 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 68475-42-3 (Anagrelide)
  • Hazard Symbols
  • Synonyms 6,7-Dichloro-1,5-dihydroimidazo[2,1-β]quinazolin-2(3H)-one;Anagrelide;Xagrid;
  • PSA 44.70000
  • LogP 1.62860

Synthetic route

anagrelide hemiformate

anagrelide hemiformate

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With water In ethanol at 23℃; for 3h;99%
ethyl (2‑amino‑5,6‑dichloroquinazoline‑3(4H)‑yl)acetate

ethyl (2‑amino‑5,6‑dichloroquinazoline‑3(4H)‑yl)acetate

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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
70406-92-7

N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester

chloroformamidine hydrochloride
29671-92-9

chloroformamidine hydrochloride

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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%
(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid ethyl ester hydrobromide

(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid ethyl ester hydrobromide

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With sodium hydrogencarbonate In water at 37℃; for 1h; pH=8 - 10; Product distribution / selectivity;
(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid methyl ester hydrochloride

(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid methyl ester hydrochloride

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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;
(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid ethyl ester hydrochloride

(2-amino-5,6-dichloroquinazolin-3(4H)-yl)acetic acid ethyl ester hydrochloride

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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
146374-56-3

ethyl-(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetate

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With hydrogenchloride; potassium carbonate In ethylene glycol
With acetic acid0.116 g (91%)
With hydrogenchloride In N-methyl-acetamide0.070 g (54.7%)
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetonitrile
146374-57-4

(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetonitrile

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With potassium carbonate In ethylene glycol
ethyl 5,6-dichloro-3,4-dihydro-2(1H)-iminoquinazoline-3-acetate hydrobromide

ethyl 5,6-dichloro-3,4-dihydro-2(1H)-iminoquinazoline-3-acetate hydrobromide

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With triethylamine In ethanol179 g (92%)
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile
146374-57-4

(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile

A

6,7-Dichioro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

6,7-Dichioro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

B

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With potassium carbonate In ethylene glycol
(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile
146374-57-4

(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetonitrile

A

6,7-Dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

6,7-Dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

B

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With potassium carbonate In ethylene glycol
ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetate
146374-56-3

ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetate

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With acetic acid0.116 g (91%)
ethyl-(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetate
146374-56-3

ethyl-(2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl) acetate

A

6,7-Dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

6,7-Dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3 H ]-one hydrochloride semihydrate

B

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With hydrogenchloride; potassium carbonate In ethylene glycol
ethyl-5,6-dichloro-3,4-dihydro-2-(1H)-iminoquinazoline-3-acetate hydrobromide
70381-75-8

ethyl-5,6-dichloro-3,4-dihydro-2-(1H)-iminoquinazoline-3-acetate hydrobromide

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With triethylamine In isopropyl alcohol for 2h; Heating / reflux;
ethyl 5,6-dichloro-3,4-dihydro-2-iminoquinazoline-3-acetate hydrobromide

ethyl 5,6-dichloro-3,4-dihydro-2-iminoquinazoline-3-acetate hydrobromide

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
With triethylamine In ethanol at 30℃; for 4h; Reflux;
4,5-Dichloro-1H-indole-2,3-dione
1677-47-0

4,5-Dichloro-1H-indole-2,3-dione

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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
20776-60-7

6-amino-2,3-dichlorobenzoic acid

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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
70380-51-7

3,4-dichloro-2-hydroxymethylaniline

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
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
70406-92-7

N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester

anagrelide
68475-42-3

anagrelide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: toluene
2: triethylamine / ethanol
View Scheme
formic acid
64-18-6

formic acid

anagrelide
68475-42-3

anagrelide

anagrelide hemiformate

anagrelide hemiformate

Conditions
ConditionsYield
In water at 60℃; for 3h;90%
ethanol
64-17-5

ethanol

anagrelide
68475-42-3

anagrelide

ethyl (2‑amino‑5,6‑dichloroquinazoline‑3(4H)‑yl)acetate

ethyl (2‑amino‑5,6‑dichloroquinazoline‑3(4H)‑yl)acetate

Conditions
ConditionsYield
With phosphoric acid at 85℃; for 18h;77.5%
anagrelide
68475-42-3

anagrelide

anagrelide hydrochloride
58579-51-4

anagrelide hydrochloride

Conditions
ConditionsYield
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;
ibuprofen
15687-27-1

ibuprofen

anagrelide
68475-42-3

anagrelide

(2S)-2-(6-methoxy(2-naphthyl))propanoic acid
22204-53-1

(2S)-2-(6-methoxy(2-naphthyl))propanoic acid

anagrelide
68475-42-3

anagrelide

anagrelide hydrochloride monohydrate

anagrelide hydrochloride monohydrate

Conditions
ConditionsYield
With hydrogenchloride; water In ethanol at 20℃; for 2h; Time; Solvent;

Anagrelide Specification

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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