HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800685Generated: November 2, 2026
Chloroacetyl chloride → HCID 59507038, compound
https://huagongshe.com/reaction/1800685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86646073 | HCID 86646073 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 59507038 | HCID 59507038 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08344135B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-f4dc536fbc524fa8adc941ba391a8f52 |
|---|
| Source note | uspto-grants-2013_01 |
|---|