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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265213Generated: October 31, 2026

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

https://huagongshe.com/reaction/2265213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,1,3-Benzothiadiazole, 4-chlorosulfonyl-HCID 2735459—
ReactantMethyl 2-Amino-4-bromobenzoateHCID 17871390—
Product2-(Benzo[1,2,5]thiadiazole-4-sulfonylamino)-4-bromo-benzoic acid methyl esterHCID 6877032675%

Reaction Steps

The title compound (3.95 g, 75%) was prepared from methyl 2-amino-4-bromobenzoate and 4-chlorosulfonyl-2,1,3-benzothiadiazole as in Example 1, Part A. MS (ESI−): mass calcd. for C14H10BrN3O4S2, 426.9; m/z found, 426 [M−H]−. 1H NMR (400 MHz, CDCl3): 11.34 (br s, 1H), 8.40 (dd, J=7.0, 0.9, 1H), 8.24 (dd, J=8.8, 0.9, 1H), 7.92 (d, J=1.8, 1H), 7.74 (dd, J=8.8, 7.0, 1H), 7.72 (d, J=8.5, 1H), 7.10 (dd, J=8.5, 1.8, 1H), 3.92 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855292B2
Source datasetuspto-grants-2010_12
ORD IDord-6f4f707d50d04fa2a475a820cf420600
Source noteuspto-grants-2010_12