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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435136Generated: October 30, 2026

Dimethylformamide → HCID 57937599, compound

https://huagongshe.com/reaction/1435136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAcetohydrazideHCID 14039—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-{4-{[(1R)-1-(2-chlorophenyl)ethyl]oxy}-5-[(methyloxy)carbonyl]-2-thienyl}-1H-benzimidazole-5-carboxylic acidHCID 68569969—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57937599HCID 5793759991.3%

Reaction Steps

A 20.0 mL flask was charged with 150 mg (0.329 mmol) of 1-{4-{[(1R)-1-(2-chlorophenyl)ethyl]oxy}-5-[(methyloxy)carbonyl]-2-thienyl}-1H-benzimidazole-5-carboxylic acid (Intermediate 34, 0.120 mL, 0.658 mmol) of diisopropyl ethylamine, 24.4 mg (0.329 mmol) of acethydrazide and 2.00 ml of DMF. Next, 125 mg (0.329 mmol) of O-(7-Aza benzotriazole-1-yl)-N,N,N′,N′ tetramethyluranium hexafluoro phosphate was added and the reaction mixture stirred at rt for 30 min. 10 mL of water and 30 mL of DCM was added and the organic layer separated. The organic layer was adsorbed onto silica gel and chromatographed to give 154 mg (91% yield) of a tan solid. MS (APCI): 513 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615643B2
Source datasetuspto-grants-2009_11
ORD IDord-252524b17ac3428a9a2e177da461c5a4
Source noteuspto-grants-2009_11