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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18612Generated: October 29, 2026

5-(5-Chlorothiophen-2-yl)isoxazol-3-ylmethyl methanesulfonate → HCID 67012730, compound

https://huagongshe.com/reaction/18612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(5-Chlorothiophen-2-yl)isoxazol-3-ylmethyl methanesulfonateHCID 86595878—
ReactantHCID 178497594HCID 178497594—
ProductHCID 67012730HCID 67012730—
Product1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-7-methyl-1H-benzoimidazole-5-carboxylic acidHCID 68616323—

Reaction Steps

1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-7-methyl-1H-benzoimidazole-5-carboxylic acid and 3-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-7-methyl-3H-benzoimidazole-5-carboxylic acid were prepared by a procedure according to example 81 starting from 200 mg (0.56 mmol) 2-(1-Cyclopropyl-piperidin-4-ylcarbamoyl)-7-methyl-1H-benzoimidazole-5-carboxylic acid methyl ester and 164.8 mg (0.56 mmol) methanesulfonic acid 5-(5-chloro-thiophen-2-yl)-isoxazol-3-ylmethyl ester. Hydrolysis of the resulting esters by treatment with LiOH and purification by preparative RP-HPLC (CH3CN/H2O gradient+0.05% formic acid) gave the title compounds as their formiates in form of white amorphous solids. Structural assignment of both isomers was achieved by NOE-spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741341B2
Source datasetuspto-grants-2010_06
ORD IDord-3ef71dcded8e4411acd2e6fd3e0c396f
Source noteuspto-grants-2010_06