Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927571Generated: October 25, 2026

Thiolan-3-amine → 3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-(tetrahydrothiophen-3-ylamino)-cyclobut-3-ene-1,2-dione

https://huagongshe.com/reaction/1927571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiolan-3-amineHCID 522918—
Reactant3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-ethoxy-cyclobut-3-ene-1,2-dioneHCID 86641802—
SolventEthanolHCID 702—
Product3-(4-Chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-(tetrahydrothiophen-3-ylamino)-cyclobut-3-ene-1,2-dioneHCID 25112996—

Reaction Steps

The title compound is prepared from 3-(4-chloro-2-hydroxy-3-methanesulfonyl-phenylamino)-4-ethoxy-cyclobut-3-ene-1,2-dione analogously to 6-chloro-2-hydroxy-N,N-dimethyl-3-{2-[(R)-1-((2R,5R)-5-methyl-tetrahydrofuran-2-yl)-propylamino]-3,4-dioxo-cyclobut-1-enylamino}-benzenesulfonamide (Example 3) by replacing (R)-1-((2R,5R)-5-methyl-tetrahydrofuran-2-yl)-propylamine p-toluenesulfonate salt with tetrahydrothiophen-3-ylamine. The reaction is carried out in EtOH. The title compound is obtained. MH+ 403.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183281B2
Source datasetuspto-grants-2012_05
ORD IDord-f81461ffc2dc43ee85f7fd900d6c25cd
Source noteuspto-grants-2012_05