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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979914Generated: October 30, 2026

Triethylamine → HCID 15614722, compound

https://huagongshe.com/reaction/979914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Furoic acidHCID 10268—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 13588033HCID 13588033—
SolventDichloromethaneHCID 6344—
ProductHCID 15614722HCID 1561472274%

Reaction Steps

To a stirred mixture of 3.14 parts of 3-furancarboxylic acid, 6 parts of N,N-diethylethanamine and 390 parts of dichloromethane were added 7.2 parts of 2-chloro-1-methylpyridinium iodide. After stirring for 10 minutes at room temperature, 7 parts of 4-[(1H-benzimidazol-2-yl)amino]-1-piperidineacetonitrile were added and the whole was stirred for 1 hour at room temperature. The reaction mixture was washed with water. The organic phase was dried, filtered and evaporated. The residue was crystallized from acetonitrile, yielding 7 parts (74%) of 4-[[1-(3-furanylcarbonyl)-1H-benzimidazol-2-yl]amino]-1-piperidineacetonitrile (129).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04634704
Source datasetuspto-grants-1987_01
ORD IDord-a37525ea407043da9e68c07560e45fa2
Source noteuspto-grants-1987_01