Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051881Generated: November 4, 2026

Acetic Anhydride → HCID 71735082, compound

https://huagongshe.com/reaction/1051881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 71737164HCID 71737164—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 71735082HCID 7173508221.5%

Reaction Steps

Acetic anhydride (0.66 g, 0.65 mmol) was added to stirred solution of 44243-azabicyclo[3.1.0]hexane-3-carbonyl)-4-(4-chlorophenyl)thiazol-5-yl)benzenesulfonamide (Compound 73, 0.3 g, 0.65 mmol) in pyridine (5 ml) at 0° C. The reaction mixture was stirred at room temperature for 2 hr. The progress of reaction was monitored by TLC. The reaction mixture was diluted with water (25 ml) and extracted with ethyl acetate (2×25 ml). The combined organic layer was dried over sodium sulphate and concentrated under reduced pressure to obtain a crude product; which was purified by flash column chromatography using 25% ethyl acetate in hexanes as an eluent to obtain the title compound (0.07 g, 21.4%). MS: m/z 502 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-13b8aed74cfe49e48367e9d6264e6185
Source noteuspto-grants-2016_07