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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265189Generated: October 31, 2026

2,1,3-Benzothiadiazole, 4-chlorosulfonyl- → 2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-methylbenzoic acid methyl ester

https://huagongshe.com/reaction/2265189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,1,3-Benzothiadiazole, 4-chlorosulfonyl-HCID 2735459—
ReactantMethyl 2-amino-4-methylbenzoateHCID 11205965—
Product2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-methylbenzoic acid methyl esterHCID 6877072553%

Reaction Steps

The title compound (1.22 g, 53%) was prepared from benzo[1,2,5]thiadiazole-4-sulfonyl chloride and 2-amino-4-methyl-benzoic acid methyl ester as in Example 10, Part A. 1H NMR (500 MHz, CDCl3): 11.28 (s, 1H), 8.36 (dd, J=7.1, 1.0, 1H), 8.19 (dd, J=8.8, 1.0, 1H), 7.73 (d, J=8.1, 1H), 7.68 (dd, J=8.8, 7.1, 1H), 7.51 (br s, 1H), 6.77 (dd, J=8.1, 0.9, 1H), 3.89 (s, 3H), 2.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855292B2
Source datasetuspto-grants-2010_12
ORD IDord-5c44e3e1eed445e0b362f640eca8d37d
Source noteuspto-grants-2010_12