Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298803Generated: October 30, 2026

HCID 18378637, compound → HCID 86758696, compound

https://huagongshe.com/reaction/2298803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18378637HCID 18378637—
ReactantHCID 86758697HCID 86758697—
ReactantHCID 178527226HCID 178527226—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86758696HCID 8675869654.3%

Reaction Steps

A mixture of 2-methoxy-4-(2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)-carbonylbenzoic acid (200 mg), 4-amino-1-tert-butoxycarbonyl-2-methyl-1H-benzimidazole (152 mg), WSCD·HCl [water soluble carbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 141 mg] and 1-hydroxybenzotiazole (100 mg) in N,N-dimethylformamide (5 ml) was stirred at room temperature overnight, and the mixture was diluted with ethyl acetate. The solution was washed successively with saturated aqueous sodium hydrogencarbonate solution, water, and brine and dried over magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography using chloroform as an eluent to give 2-methoxy-N-[2-methyl-1-(tert-butoxycarbonyl)-1H-benzimidazol-4-yl]-4-(2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl)-carbonylbenzamide (185 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495542B1
Source datasetuspto-grants-2002_12
ORD IDord-9a7a0bb4eff347b29defd26a4f3e34bd
Source noteuspto-grants-2002_12