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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244342Generated: October 27, 2026

Ammonium trifluoroacetate → 4-methoxy-2-[5-(3-methyl-benzo[b]thiophen-2-yl)-1H-imidazol-2-yl]-7-morpholin-4-yl-benzothiazole

https://huagongshe.com/reaction/1244342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium trifluoroacetateHCID 2724268—
Reactant4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid [2-(3-methyl-benzo[b]thiophen-2-yl)-2-oxo-ethyl]-amideHCID 21137076—
SolventWaterHCID 962—
Product4-methoxy-2-[5-(3-methyl-benzo[b]thiophen-2-yl)-1H-imidazol-2-yl]-7-morpholin-4-yl-benzothiazoleHCID 2191921252.1%

Reaction Steps

A mixture of 0.16 g 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid [2-(3-methyl-benzo[b]thiophen-2-yl)-2-oxo-ethyl]-amide and 0.44 g ammonium triflouroacetate was melted at 180° C. for 45 minutes and, after cooling to room temperature, suspended in water. Extraction with dichloromethane and chromatography on silicagel with ethylacetate/hexane 1:1 gave 0.08 g (51%) 4-methoxy-2-[5-(3-methyl-benzo[b]thiophen-2-yl)-1H-imidazol-2-yl]-7-morpholin-4-yl-benzothiazole as yellow solid; M.p.: 213–215° C.; MS (ISP): m/e=463 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-84a449fad0d0452989f4eaf1bc19a57f
Source noteuspto-grants-2006_10