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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631075Generated: November 3, 2026

Triethylamine → 3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxy-N-(3-methoxyphenyl)-propanamide

https://huagongshe.com/reaction/1631075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-MethoxyanilineHCID 10824—
ReactantThionyl ChlorideHCID 24386—
Reactant3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxypropanoic acidHCID 58097206—
SolventDichloromethaneHCID 6344—
Product3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxy-N-(3-methoxyphenyl)-propanamideHCID 4685120948%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(3,6-Dibromo-9H-carbazol-9-yl)-2-hydroxypropanoic acid (0.025 g, 0.061 mmol) was suspended in anhydrous CH2Cl2 and cooled to 0° C. Thionyl chloride (0.005 mL, 0.073 mmol) was added dropwise and the reaction was stirred at 0° C. for 1 h. m-Anisidine (0.008 mL, 0.073 mmol) and Et3N (0.010 mL, 0.073 mmol) were added and the reaction was allowed to warm to ambient temperature over 2.5 h. Upon completion, the solution was partitioned between EtOAc and H2O. The aqueous layer was washed 3× with EtOAc, and the combined organics were washed with saturated aqueous NaCl, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by chromatography (SiO2, 0-30% EtOAc/Hexane) to afford the desired product (15 mg, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791149B2
Source datasetuspto-grants-2014_07
ORD IDord-3482d8b693fb415dbf930b2bad90d80a
Source noteuspto-grants-2014_07