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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068929Generated: November 1, 2026

Benzene, 1-chloro-3-isocyanato- → HCID 178522045, compound

https://huagongshe.com/reaction/1068929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-chloro-3-isocyanato-HCID 17968—
Reactant1H-pyrazolo(4,3-d)pyrimidineHCID 21083976—
ReactantHCID 178509242HCID 178509242—
SolventEthanolHCID 702—
Solvent1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178522045HCID 178522045—

Reaction Conditions

Temperature60 °C

Reaction Steps

With the exclusion of moisture, 261 mg (1.00 mmol) of 3-amino-4-(3-chlorophenylamino)-1H-pyrazolo[3,4-d]pyrimidine (see Step 1.6) are dissolved in 2.5 ml of dioxane and 1 ml of DMEU; 137 I (1.1 mmol) of 3-chloro-phenyl isocyanate are added and the reaction mixture is stirred overnight at RT and finally for 16 hours at 60° C. Since, according to HPLC, not all of the pyrazolo-pyrimidine has reacted, a further 40 all of 3chloro-phenyl isocyanate are added and the mixture is stirred for a further 20 hours at 60° C. Working-up analogously to Example 66 and stirring in hot ethanol yield 4-(3-chloro-phenylamino)-3-[(3-chloro-phenyl-amino)-carbonylamino]-1H-pyrazolo[3,4-d]pyrimidine; HPLC: tRet(grad20-100)=12.4; FARMS: (M+H)+=414.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251911B1
Source datasetuspto-grants-2001_06
ORD IDord-00d32a0937114bddbc63717e4348ee98
Source noteuspto-grants-2001_06