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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(5-Chlorothiophen-2-yl)isoxazol-3-ylmethyl methanesulfonate | HCID 86595878 | — |
| Reactant | HCID 178497594 | HCID 178497594 | — |
| Product | HCID 67012730 | HCID 67012730 | — |
| Product | 1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-2-(1-cyclopropyl-piperidin-4-ylcarbamoyl)-7-methyl-1H-benzoimidazole-5-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741341B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-3ef71dcded8e4411acd2e6fd3e0c396f |
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| Source note | uspto-grants-2010_06 |
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