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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470641Generated: October 25, 2026

Water → 2-biphenyl-4-yl-1H-indole-7-carboxylic acid

https://huagongshe.com/reaction/1470641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Amino-3-biphenyl-4-ylethynyl-benzoic acid methyl esterHCID 66706342—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-biphenyl-4-yl-1H-indole-7-carboxylic acidHCID 4694698750.9%

Reaction Steps

To a cold solution of 2-amino-3-biphenyl-4-ylethynyl-benzoic acid methyl ester (300 mg, 0.91 mmol) in NMP (5 mL) was added dropwise a solution of potassium t-butoxide (205 mg, 1.83 mmol) in NMP (5 mL). This reaction mixture was allowed to stir at room temperature for 5 h. After the reaction is completed it was poured into water and pH was adjusted to 2. The resulting precipitate was collected by filtration and was washed with water. Finally it was dried in a vacuum oven to get the 145 mg of 2-biphenyl-4-yl-1H-indole-7-carboxylic acid as a pale yellow coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006454B2
Source datasetuspto-grants-2015_04
ORD IDord-0044159c5c9c4c7790a13c638054f69b
Source noteuspto-grants-2015_04