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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531591Generated: October 27, 2026

Triethylamine → N-[4-(2,4,6-Trimethylphenyl)-2-thiazolyl]-1-tert-butoxycarbonyl-indoline-2-carboxamide

https://huagongshe.com/reaction/1531591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantIndoline-2-carboxylic acid, N-BOC protectedHCID 2794663—
Reactant4-Mesitylthiazol-2-amine hydrobromideHCID 16896300—
SolventDimethylformamideHCID 6228—
ProductN-[4-(2,4,6-Trimethylphenyl)-2-thiazolyl]-1-tert-butoxycarbonyl-indoline-2-carboxamideHCID 2124948295%

Reaction Steps

21 g of 1-tert-butoxycarbonyl-indoline-2-carboxylic acid, then 35.2 g of 1-benzotriazolyl-oxytris (dimethylamino)phosphonium hexafluorophosphate (BOP) and the then 24.2 g of triethylamine are added successively to a solution of 23.5 g of 2-amino-4-(2,4,6-trimethylphenyl)thiazole hydrobromide in 250 ml of dimethylformamide. The reaction mixture is stirred at ambient temperature for 12 h. The solvent is then evaporated under reduced pressure and 150 ml of ethyl acetate are poured onto the residue. The organic solution is washed with a saturated aqueous NaCl solution and dried over anhydrous magnesium sulphate. The solid obtained after evaporation of the solvent is washed with diisopropyl ether. Yield: 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037094E1
Source datasetuspto-grants-2001_03
ORD IDord-0c5122198e3a4eed9b38fbfde60d31a1
Source noteuspto-grants-2001_03