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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371456Generated: November 2, 2026

Methanesulfonyl chloride → n-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-n'-{[1-(methylsulfonyl)piperidin-4-yl]methyl}urea

https://huagongshe.com/reaction/1371456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 69507286HCID 69507286—
SolventDichloromethaneHCID 6344—
Productn-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-n'-{[1-(methylsulfonyl)piperidin-4-yl]methyl}ureaHCID 69507201—

Reaction Conditions

Temperature23 °C

Reaction Steps

Methane sulphonyl choride (0.013 ml) was added to a solution of Intermediate 18 (0.054 g) and N,N-diisopropylethylamine (0.063 ml) in dichloromethane (2 ml). The solution was stirred for 16 h at 23° C. The solvent was removed in vacuo and the residue purified by solid phase extraction (Isolute SCX sulphonic acid column) eluting with methanol followed by 10% 0.880 ammonia solution in methanol, to give the title compound as a clear gum (0.035 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157457B2
Source datasetuspto-grants-2007_01
ORD IDord-0c256e7cbc6844368cb96c9e2f7c8605
Source noteuspto-grants-2007_01