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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531307Generated: November 3, 2026

{5-[(6-Methyl-4'-trifluoromethylbiphenyl-2-carbonyl)-amino]-indan-2-yl}-carbamic acid tert-butyl ester → 6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide

https://huagongshe.com/reaction/1531307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{5-[(6-Methyl-4'-trifluoromethylbiphenyl-2-carbonyl)-amino]-indan-2-yl}-carbamic acid tert-butyl esterHCID 69700046—
SolventFormic AcidHCID 284—
Product6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amideHCID 22498815—

Reaction Steps

A solution of {5-[(6-methyl-4′-trifluoromethylbiphenyl-2-carbonyl)-amino]-indan-2-yl}-carbamic acid tert-butyl ester (5.19 g,10.5 mmol) in formic acid (40 mL) is heated to 40° C. with stirring. After 3 h, the reaction mixture is cooled to room temperature and stirring is continued for 16 h. The reaction mixture is concentrated under reduced pressure and the resulting oil dissolved in ethyl acetate. The organic layer is washed with 8% NaHCO3 solution until the aqueous layer remains basic at which point a precipitate forms in the organic layer. The precipitate is collected by filtration to give 6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197798B1
Source datasetuspto-grants-2001_03
ORD IDord-2b0875f01446478cbd93c4bbd0f1b16a
Source noteuspto-grants-2001_03