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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195737Generated: October 25, 2026

Benzoyl chloride → 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/2195737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(4-amino-benzyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 69447499—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 6945303783%

Reaction Steps

A solution of 3-(4-amino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (62 mg, 0.21 mmol), DIPEA (0.06 mL, 0.32 mmol), benzoyl chloride (0.03 mL, 0.23 mmol) and THF (5 mL) was stirred for 10 hr at room temperature. The solution was then diluted with ether (20 mL) and ethyl acetate (20 mL) and washed with aq. NaHCO3 (50 mL). The organic layer was dried over MgSO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane, 2:3) to provide 3-(4-benzoylamino-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (69 mg, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338416B2
Source datasetuspto-grants-2012_12
ORD IDord-66b5bdfad6f74307aa75b204d7fb955f
Source noteuspto-grants-2012_12