HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531270Generated: October 31, 2026
{5-[(4'-Trifluoromethylbiphenyl-2-carbonyl)-amino]indan-2-yl}-carbamic acid tert-butyl ester → 4'-Trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide
https://huagongshe.com/reaction/1531270
Participants
| Role | Name | HCID | Charge |
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| Reactant | {5-[(4'-Trifluoromethylbiphenyl-2-carbonyl)-amino]indan-2-yl}-carbamic acid tert-butyl ester | HCID 70184229 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 4'-Trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide | HCID 21253382 | — |
Reaction Steps
A solution of the title E compound ({5-[(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 4′-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide. The organic layer of the filtrate is dried (MgSO4) and concentrated under reduced pressure to give a solid. Trituation of the solid with diethyl ether yields additional 4′-trifluoromethylbiphenyl-2-carboxylic acid (2-amino-indan-5-yl)-amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197798B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-adaa41867d2c48c5a603e00a2e8b2ea3 |
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| Source note | uspto-grants-2001_03 |
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