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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197822Generated: October 25, 2026

Dimethylformamide → ethyl 4-[[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1197822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
Reactant1-Piperidinecarboxylic acid, 4-(1H-benzimidazol-2-ylamino)-, ethyl esterHCID 3018455—
Reactant5-(Bromomethyl)-2-methyloxazoleHCID 12808786—
SolventWaterHCID 962—
Productethyl 4-[[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylateHCID 1910506011.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 23 parts of 5-(bromomethyl)-2-methyloxazole, 57.6 parts of ethyl 4-[(1H-benzimidazol-2-yl)amino]-1-piperidinecarboxylate, 26.5 parts of sodium carbonate and 470 parts of N,N-dimethylformamide was stirred for 18 hours at 80° C. The reaction mixture was poured into water and the whole was extracted with 4-methyl-2-pentanone. The extract was washed with water, dried, filtered and evaporated. The residue was stirred in acetonitrile. The precipitate was filtered off and the filtrate was evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 90:10). The eluent of the desired fraction was evaporated, yielding 6 parts (11.2%) of ethyl 4-[[1-[(2-methyl-5-oxazolyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate (comp. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278165
Source datasetuspto-grants-1994_01
ORD IDord-a9d81ef28dee4c71a3f4be4cfe4f67ab
Source noteuspto-grants-1994_01