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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430702Generated: October 29, 2026

Methanesulfonyl chloride → HCID 18346038, compound

https://huagongshe.com/reaction/430702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 18346039HCID 18346039—
CatalystAdams' catalystHCID 345198—
ProductHCID 18346038HCID 18346038—

Reaction Steps

Proceeding as described in Example 13 above, but substituting 3-methoxyphenylisocyanate with 3-nitrophenylisocynate gave 1-{1-(R)-[4-(3,4-dichlorobenzyl)-piperidin-1-ylmethyl]-2-methylpropyl}-3-(3-nitrophenyl)urea which was then converted to the corresponding 1-{1-(R)-[4-(3,4-dichlorobenzyl)piperidin-1-ylmethyl]-2-methylpropyl}-3-(3-aminophenyl)urea under catalytic hydrogenation conditions using PtO2 catalyst, followed by reaction with methylsulfonyl chloride to give 1-{1-(R)-[4-(3,4-dichlorobenzyl)-piperidin-1-ylmethyl]-2-methylpropyl}-3-(3-methylsulfonylaminophenyl)urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323223B1
Source datasetuspto-grants-2001_11
ORD IDord-b8c10415f5ab48e48bc837f6749912ea
Source noteuspto-grants-2001_11