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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225451Generated: October 30, 2026

3,5-Dichloro-2-hydroxybenzenesulphonyl chloride → 3-(3,5-Dichloro-2-hydroxybenzenesulfonamido)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol

https://huagongshe.com/reaction/2225451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
Reactant1-[3-Amino-2-(2,4-dichlorophenyl)-2-hydroxyprop-1-yl]-1H-1,2,4-triazoleHCID 14706521—
Product3-(3,5-Dichloro-2-hydroxybenzenesulfonamido)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-olHCID 18957972—

Reaction Steps

Following the procedure described in the preceeding examples but using 2-(2,4-dichlorophenyl)-3-amino-1-(1H-1,2,4-triazol-1-yl)propan-2-ol and 3,5-dichloro-2-hydroxybenzenesulfonylchloride, the title compound was obtained in a similar yield: mp dec; 1H NMR (80 MHz, MeOH-d4)δ(TMS) 8.4-8.1 (m, arom), 7.7-7.4 (m, CH=N, arom), 7.3-7.0 (m, arom), 4.76 (AB system, Δv=0.35, J=14.5 Hz, 2H, CH2 -Tr), 3.81 (AB system, Δv=0.72, J=14 Hz, 2H, CH2NH). Anal calcd. for C17H14Cl4N4O4S: C 39.87%; H 2.76%; N 10.94%. Found: C 39.75%; H 2.96%; N 10.90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344839
Source datasetuspto-grants-1994_09
ORD IDord-601c64183cdc468dbd2716b9cfe31acc
Source noteuspto-grants-1994_09