Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29607Generated: October 28, 2026

4-t-Butylbenzenesulfonyl chloride → HCID 59788678, compound

https://huagongshe.com/reaction/29607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
Reactant(2-Amino-5-chloro-phenyl)-(3-methyl-[1,2,3]triazol-4-yl)methanoneHCID 59788757—
SolventPyridineHCID 1049—
ProductHCID 59788678HCID 59788678—

Reaction Steps

Following the general procedure for synthesis of N-arylbenzenesulfonamides, 28 mg (0.12 mmol) of (2-Amino-5-chloro-phenyl)-(3-methyl-[1,2,3]triazol-4-yl)methanone and 56 mg (0.24 mmol) of 4-tert-butylphenylsulfonyl chloride were combined in 0.5 ml of anhydrous pyridine at 60° C. to give, after purification, the title product as a pale yellow solid: 1H NMR CD3OD δ (ppm): 1.20 (s, 9H), 4.15 (s, 3H), 7.37 (d, 2H), 7.52 (d, 2H), 7.59-7.62 (m, 2H), 8.27 (d, 1H), 8.53 (s, 1H); MS: (M+H)/z=433.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420055B2
Source datasetuspto-grants-2008_09
ORD IDord-297a2dce5427401bb9f5d613e67c3e29
Source noteuspto-grants-2008_09