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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080778Generated: November 2, 2026

2,6-Lutidine → Methyl 4-[6-(cyclopentyloxycarbonyl)aminobenzimidazol-1-ylmethyl]-3-methoxybenzoate

https://huagongshe.com/reaction/1080778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantCyclopentyl chloroformateHCID 2735892—
ReactantMethyl 4-(6-aminobenzimidazol-1-ylmethyl)-3-methoxybenzoateHCID 14763098—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-[6-(cyclopentyloxycarbonyl)aminobenzimidazol-1-ylmethyl]-3-methoxybenzoateHCID 1476309993%

Reaction Steps

A solution of methyl 4-(6-aminobenzimidazol-1-ylmethyl)-3-methoxybenzoate (J) (0.63 g.) and 2,6-lutidine (0.36 ml.) in dichloromethane (10 ml.) was treated with cyclopentyl chloroformate (0.33 g.). After stirring for 24 hours the solution was diluted with dichloromethane. The mixture was washed successively with 20% w/v sodium hydroxide, water, and brine, then dried (MgSO4) and evaporated. The resultant residue was purified by flash chromatography on a 6×20 cm. silica gel column using 1:3 v/v hexane:ethyl acetate as the eluent to give the title compound (0.57 g., 93%); NMR: 1.7[m,8H, (CH2)4 ], 3.8(s,3H, OCH3), 3.9(s,3H, OCH3) 5.2(m, 1H, CHO), 6.17-7.0(br m,3H), 7.5-7.8(br m,4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583152
Source datasetuspto-grants-1996_12
ORD IDord-12e6fb457f794ccaa283e3b017fd2ab4
Source noteuspto-grants-1996_12