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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191330Generated: November 1, 2026

Triethylamine → N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide

https://huagongshe.com/reaction/1191330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactant(2-Amino-4,5-dimethoxy-phenyl)-(3-bromo-phenyl)-methanoneHCID 7148514—
SolventNitrogenHCID 947—
SolventDichloromethaneHCID 6344—
ProductN-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamideHCID 66849274—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2-amino-4,5-dimethoxyphenyl)(3-bromophenyl)methanone (5 g, 14.9 mmol) in dry DCM (125 mL) was added thiophen-2-ylacetic acid (2.54 g, 17.9 mmol) and Et3N (6.77, 66.9 mmol) at 0° C. in N2. 10 minutes later, POCK (3.4 g, 22.31 mmol) was added dropwise at 0° C. in N2. The reaction mixture was stirred for 1 hour at 0° C. and then quenched with saturated NaHCO3, and neutralized to pH=8. The mixture was exacted with ACM (30 mL×3). The combined organic layer was dried over anhydrous MgSO4, filtered and concentrated under vacuum to afford N-{2-[(3-bromophenyl)carbonyl]-4,5-dimethoxyphenyl}-2-(thiophen-2-yl)acetamide. MS (M+H)=460 and 462.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680116B2
Source datasetuspto-grants-2014_03
ORD IDord-f6e5b460fdec4f8bb7b766f39a88414e
Source noteuspto-grants-2014_03