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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789354Generated: October 27, 2026

Methanesulfonyl isocyanate → HCID 13768039, compound

https://huagongshe.com/reaction/1789354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl isocyanateHCID 12668338—
ReactantHCID 13768101HCID 13768101—
SolventAcetoneHCID 180—
ProductHCID 13768039HCID 1376803961.3%

Reaction Steps

1.94 g of 2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazolidine are dissolved in anhydrous acetone, and 0.73 g of methanesulfonyl isocyanate is added thereto at room temperature. After the mixture is stirred for 30 minutes, the mixture is concentrated under reduced pressure to remove solvent. The residue is collected by filtration, and washed with water and ether, successively. The crude product thus obtained is recrystallized from a mixture of acetone and ether. 1.56 g of N-methanesulfonyl-2-{2-[2-(4-(3-fluorophenyl)piperazin-1-yl)ethyloxy]phenyl}thiazollidine-3-carboxamide are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689327
Source datasetuspto-grants-1987_08
ORD IDord-4309e47a359d4d8aa7980c2c2a42a140
Source noteuspto-grants-1987_08