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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442550Generated: November 1, 2026

Acetic Acid → HCID 58679113, compound

https://huagongshe.com/reaction/1442550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium AcetateHCID 517045—
ReactantHCID 58679084HCID 58679084—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58679113HCID 58679113110.9%

Reaction Steps

To a suspension of methyl 5-(2-amino-4-benzyloxyphenyl)-6-cyclohexyl-4H-thieno[3,2-b]pyrrole-2-carboxylate (6.30 g, 13.8 mmol), sodium acetate (1.36 g, 16.6 mmol) and acetic acid (0.95 ml, 16.6 mmol) in tetrahydrofuran (100 ml) was added dropwise chloroacetyl chloride (1.32 ml, 16.6 mmol), and the mixture was stirred at room temperature for 2 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium hydrogen carbonate solution, saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the solvent was evaporated under reduced pressure. The obtained crude product of methyl 5-[4-benzyloxy-2-(2-chloroacetylamino)phenyl]-6-cyclohexyl-4H-thieno[3,2-b]pyrrole-2-carboxylate (8.22 g) was used for Step 6 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659263B2
Source datasetuspto-grants-2010_02
ORD IDord-d71ff88977d24db38df1525024a94b9d
Source noteuspto-grants-2010_02