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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518048Generated: November 5, 2026

Acetic Anhydride → HCID 178502000, compound

https://huagongshe.com/reaction/1518048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178501999HCID 178501999—
SolventDichloromethaneHCID 6344—
ProductHCID 178502000HCID 17850200080.2%

Reaction Steps

To a solution of 7-amino-5-(methoxycarbonyl)amino-2-(4-bromophenyl)-1H-benzo[d]-imidazole (60 mg, 0.17 mmol) in dichloromethane (5 mL) was added acetic anhydride (18 mg, 0.17 mmol) and the solution was stirred at room temperature for 3 h. The reaction mixture was concentrated in vacuo and purified by column chromatography on silica gel using hexane/EtOAc (4/1) as the eluant to afford the desired product (55 mg, 80%) as a pale yellow powder: 1H-NMR (300 MHz, CD3OD) δ 2.24 (s, 3H), 3.74 (s, 3H), 7.65 (m, 3H), 7.67 (bs, 1H), 7.90 (m, 2H); ESI MS m/z 403.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232410B2
Source datasetuspto-grants-2012_07
ORD IDord-135b26e731ad45a9882789d8a44d46c3
Source noteuspto-grants-2012_07