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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800685Generated: November 2, 2026

Chloroacetyl chloride → HCID 59507038, compound

https://huagongshe.com/reaction/1800685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86646073HCID 86646073—
SolventDimethylacetamideHCID 31374—
ProductHCID 59507038HCID 5950703888%

Reaction Steps

To a solution of N-{3-[(2-amino[1,3]thiazolo[5,4-d]pyrimidin-5-yl)(methyl)amino]phenyl}-3-(1-cyano-1-methylethyl)benzamide (800 mg, 1.80 mmol) produced in Example D5(i) in N,N-dimethylacetamide (15 mL) was added chloroacetyl chloride (356 μL, 4.50 mmol), and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution (60 mL), and the mixture was extracted with ethyl acetate (60 mL, 10 mL). The combined organic layer was washed with saturated brine (10 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=60/40→30/70), and the fractions containing the object product were concentrated under reduced pressure. The obtained residue was recrystallized from ethyl acetate to give the title compound (823 mg, 88%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-f4dc536fbc524fa8adc941ba391a8f52
Source noteuspto-grants-2013_01