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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769102Generated: October 31, 2026

Triethylamine → 2-[(1-Acetyl-2-indolyl)carbonylamino]-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole

https://huagongshe.com/reaction/1769102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1-acetylindole-2-carboxylic AcidHCID 10219867—
Reactant2-Amino-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazoleHCID 18946571—
SolventDichloromethaneHCID 6344—
Product2-[(1-Acetyl-2-indolyl)carbonylamino]-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazoleHCID 18946565—

Reaction Steps

1.5 g of 2-amino-4-(2,4-dimethoxyphenyl)-5-ethoxycarbonylmethylthiazole, 1 g of 1-acetylindole-2carboxylic acid, 0.7 ml of triethylamine and 2.39 g of BOP are dissolved in 15 ml of dichloromethane. The reaction mixture is stirred overnight at room temperature and then concentrated under vacuum. The residue is taken up in ethyl acetate and the solution is successively washed with a buffer solution, pH=2, with a 5% solution of NaHCO3 and with water, and then the organic phase is dried over MgSO4 and concentrated under vacuum. The residue is purified by chromatography on a silica gel, eluent: dichloromethane/ethyl acetate 100/2.5 (v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380736
Source datasetuspto-grants-1995_01
ORD IDord-7ff815a8f92f4e508c8ccc0a5f2a4474
Source noteuspto-grants-1995_01