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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244297Generated: November 3, 2026

1,1'-Carbonyldiimidazole → HCID 178492012, compound

https://huagongshe.com/reaction/1244297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantAmmonium trifluoroacetateHCID 2724268—
Reactant2-Amino-1-(thiophen-2-yl)ethan-1-one hydrochlorideHCID 12609833—
Reactant4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-oxo-2-thiophen-2-yl-ethyl)-amideHCID 21137056—
SolventTriethylamineHCID 8471—
ProductHCID 178492012HCID 178492012—

Reaction Steps

In accordance with scheme 2,4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (for R1=morpholinyl, XII) and CDI (1,1′-carbonyl-diimidazole) was stirred at room temperature for about 1.5 hours. Then, for example, 2-amino-1-(2-thienyl)ethanone hydrochloride (for R3=thienyl) and triethylamine were added and stirring are continued over night at room temperature. Then a mixture of the obtained 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboxylic acid (2-oxo-2-thiophen-2-yl-ethyl)-amide (III) and ammonium triflouroacetate was melted at about 165° C. for 60 minutes to obtain 4-methoxy-7-morpholin-4-yl-2-(4-thiophen-2-yl-1H-imidazol-2-yl)-benzothiazole (Ia1 for R1=morpholinyl and R3=thienyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122545B2
Source datasetuspto-grants-2006_10
ORD IDord-d8bb2bc06f1a4a8db4b5ddfcbe2cf038
Source noteuspto-grants-2006_10