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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225457Generated: November 1, 2026

2-Acetamido-1,3-thiazole-5-sulfonyl chloride → 3-(2-Acetamido-5-thiazolesulfonamido)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol

https://huagongshe.com/reaction/2225457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Acetamido-1,3-thiazole-5-sulfonyl chlorideHCID 350261—
Reactant1-[3-Amino-2-(2,4-dichlorophenyl)-2-hydroxyprop-1-yl]-1H-1,2,4-triazoleHCID 14706521—
Product3-(2-Acetamido-5-thiazolesulfonamido)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-olHCID 18958015—

Reaction Steps

Following the procedure described in the preceeding examples but using 3-amino-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol and 2-acetamido-5-thiazolesulfonylchloride, the title compound was obtained in a similar yield: mp 96°-112° C.; 1H NMR (80 MHz, MeOH-d4)δ(TMS) 8.27 (s, 1H, CH=N), 7.74 (s, 1H, CH=N), 7.55 (d, J=8.5 Hz, 1H, arom), 7.3-7.1 (m, 2H, arom), 4.80 (AB system, Δv=0.35, J=14.5 Hz, 2H, CH2 -Tr), 3.74 (AB system, Δv=0.36, J=13.8Hz, 2H, CH2NH), 2.37 (s, 1H, Me), 2.22 (s, 1H, Me). Anal calcd. for C17H18Cl2N6O4S2 : C 40.40%; H 3.59%; N 16.63%. Found: C 40.69%; H 4.06%; N 16.70 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344839
Source datasetuspto-grants-1994_09
ORD IDord-514a39e323da47559be1fa22141ea0de
Source noteuspto-grants-1994_09