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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244334Generated: October 30, 2026

Triethylamine → 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-benzo[b]thiophen-3-yl-2-oxo-ethyl)-amide

https://huagongshe.com/reaction/1244334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acidHCID 21919216—
Reactant2-Amino-1-benzo[b]thiophen-3-yl-ethanone hydrochlorideHCID 21919260—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-benzo[b]thiophen-3-yl-2-oxo-ethyl)-amideHCID 8659500444.1%

Reaction Steps

0.30 g 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid and 0.19 g 1,1′-carbonyl-diimidazole in 6 ml DMF were stirred at room temperature for 4 hours. 0.26 g 2-amino-1-benzo[b]thiophen-3-yl-ethanone hydrochloride and 0.–16 ml triethylamine were added and stirring was continued for two days at room temperature. 100 ml water was added and the mixture was extracted with ethylacetate. The precipitate was filtered to yield 0.21 g (44%) 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-benzo[b]thiophen-3-yl-2-oxo-ethyl)-amide as a yellow solid; M.p.: 256–258° C.; MS (ISP): m/e=468 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-8c2acf689c0d46e4a1acd6d4126dda66
Source noteuspto-grants-2006_10