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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114561Generated: October 26, 2026

HCID 178503501, compound → HCID 178503484, compound

https://huagongshe.com/reaction/2114561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178503501HCID 178503501—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
ProductHCID 178503484HCID 178503484—

Reaction Conditions

Temperature80 °C

Reaction Steps

200 mg of 4-chloro-3-(2-chloro-phenyl)-6-methyl-1H-pyrazolo[3,4-d]pyrimidine (from step 4 of Example 1) was dissolved in 5 ml of 7N ammonia in methanol, and the solution was stirred at 80° C. over night in a sealed tube. The resulting reaction mixture was concentrated under vacuum and then extracted in 60 ml ethylacetate. The solution was washed first with water and next with brine, dried and after removing the solvent in vacuo afforded 190 mg (90%)) of 3-(2-chloro-phenyl)-6-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidin-4ylamine as a light tan solid, MS: 292 (M+H). The crude 3-(2-chloro-phenyl)-6-methylsulfanyl-1H-pyrazolo[3,4-d]pyrimidin-4ylamine was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435731B2
Source datasetuspto-grants-2008_10
ORD IDord-9196fa8e37974dde8d644c7c7066ea8a
Source noteuspto-grants-2008_10