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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225456Generated: November 2, 2026

2-Thiophenesulfonyl chloride → 2-(2,4-Dichlorophenyl)-3-(2-thiophenesulfonamido)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol

https://huagongshe.com/reaction/2225456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant1-[3-Amino-2-(2,4-dichlorophenyl)-2-hydroxyprop-1-yl]-1H-1,2,4-triazoleHCID 14706521—
Product2-(2,4-Dichlorophenyl)-3-(2-thiophenesulfonamido)-1-(1H-1,2,4-triazol-1-yl)propan-2-olHCID 18958023—

Reaction Steps

Following the procedure described in the preceeding example but using 3-amino-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol and 2-thienylsulfonylchloride, the title compound was obtained in a similar yield: mp 169°-180° C.; 1H NMR (80 MHz, MeOH-d4)δ(TMS) 8.19 (s, 1H, CH=N), 7.74 (s, 1H, CH=N), 7.7-7.0 (m, 6H, arom), 4-95 (AB system, Δv=0.60, J=14.5 Hz, 2H, CH2 -Tr), 3.68 (AB system, Δv=0.13, J=14 Hz, 2H, CH2NH). Anal calcd. for C15H14Cl2N4O3S2 : C 41.58%; H 3.26%; N 12.93%. Found: C 42.39%; H 3.27%; N 13.06%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344839
Source datasetuspto-grants-1994_09
ORD IDord-369ed9ab7e5c4981a8e83d3957e3a71f
Source noteuspto-grants-1994_09