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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081504Generated: October 31, 2026

2-Aminothiazole → 3-Cyclohexyl-5-ethoxy-1,3-dihydro-1-[2-methoxy-4-[N-(thiazol-2-yl)carbamoyl]benzenesulfonyl]-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1081504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
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-(thiazol-2-yl)carbamoyl]benzenesulfonyl]-2H-benzimidazol-2-oneHCID 233642407.7%

Reaction Steps

This compound is prepared by the procedure described in EXAMPLE 100 starting from 1 g of the compound obtained in EXAMPLE 13, 0.3 g of 2-aminothiazole, 1.2 g of BOP, 1 ml of DIPEA and 20 ml of DCM. It is chromatographed on silica using a DCM/MeOH mixture (99.5/0.5; v/v) as the eluent to give 0.09 g of the expected product after crystallization from EtOH. M.p.=213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05585394
Source datasetuspto-grants-1996_12
ORD IDord-6787cfcd67a347da968d5949d2ed0440
Source noteuspto-grants-1996_12