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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081501Generated: November 1, 2026

2-Butanamine, 2-methyl- → 3-Cyclohexyl-5-ethoxy-1,3-dihydro-1-[2-methoxy-4-[N-(1,1-dimethylpropyl)carbamoyl]benzenesulfonyl]-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1081501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butanamine, 2-methyl-HCID 68986—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant5-Ethoxy-1,3-dihydro-1-(2-methoxy-4-carboxybenzenesulfonyl)-3-cyclohexyl-2H-benzimidazol-2-oneHCID 15229042—
SolventDichloromethaneHCID 6344—
Product3-Cyclohexyl-5-ethoxy-1,3-dihydro-1-[2-methoxy-4-[N-(1,1-dimethylpropyl)carbamoyl]benzenesulfonyl]-2H-benzimidazol-2-oneHCID 23364273—

Reaction Steps

A mixture of 1.09 g of the compound obtained in EXAMPLE 13, 1 ml of 1,1-dimethylpropylamine, 1.2 g of BOP, 1 ml of DIPEA and 20 ml of DCM is stirred for 2 hours at RT. The reaction mixture is evaporated under vacuum, the residue is extracted with AcOEt, washed with a 1N solution of HCl, with a 1N solution of NaOH and with water and dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using a DCM/AcOEt mixture (99/1; v/v) as the eluent to give 0.88 g of the expected product in the form of white crystals. M.p.=219° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05585394
Source datasetuspto-grants-1996_12
ORD IDord-1a70902aca5941988f78041b3fc8cba6
Source noteuspto-grants-1996_12