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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492116Generated: October 30, 2026

Benzenesulfonic Acid → 4-({[({[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}amino)carbonyl]amino}methyl)benzamide benzenesulfonate dihydrate

https://huagongshe.com/reaction/492116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonic AcidHCID 7371—
Reactant4-({[({[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}amino)carbonyl]amino}methyl) benzamide hydrateHCID 69069597—
SolventIsopropanolHCID 3776—
Product4-({[({[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}amino)carbonyl]amino}methyl)benzamide benzenesulfonate dihydrateHCID 86604671—

Reaction Steps

The slurry of Description 9 was cooled to 50±3° and isopropanol (30 ml) added, followed by an aqueous solution of benzene sulfonic acid (32% w/v, 10 ml). The mixture was cooled to 22±3° over ca 1 h, seeded with authentic 4-({[({[(2S)-4-(3,4-dichlorobenzyl)morpholin-2-yl]methyl}amino)carbonyl]amino}methyl) benzamide hydrate and aged at 22±3° for 72 h. The mixture was cooled to 0±3° over 1 h and filtered. The filter cake was washed with a 4:1:0.1 mixture of isopropyl acetate/isopropyl alcohol/water (2.5 ml) and dried in vacuo at 25±5° to give the title compound as a white solid (6.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531651B2
Source datasetuspto-grants-2009_05
ORD IDord-bc381bbcb1f2457d8c416961da710763
Source noteuspto-grants-2009_05