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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397950Generated: November 1, 2026

2-Amino-6-methylbenzothiazole → 3-(indolin-1-ylsulfonyl)-N-(6-methylbenzo[d]thiazol-2-yl)benzamide

https://huagongshe.com/reaction/1397950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-methylbenzothiazoleHCID 17335—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(2,3-dihydro-1H-indole-1-sulfonyl)benzoic acidHCID 3807505—
SolventDimethylformamideHCID 6228—
Product3-(indolin-1-ylsulfonyl)-N-(6-methylbenzo[d]thiazol-2-yl)benzamideHCID 26219003—

Reaction Steps

3-(indolin-1-ylsulfonyl)benzoic acid (3) (200 mg, 0.66 mmol) and 6-methylbenzo[d]thiazol-2-amine (90 mg, 0.55 mmol) in DMF (4 mL) was added DIPEA (213 mg, 1.65 mmol) and pybop (429 mg, 0.82 mmol). using method C. The residue was purified using flash chromatography eluting with 0-30% EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give 3-(indolin-1-ylsulfonyl)-N-(6-methylbenzo[d]thiazol-2-yl)benzamide as a white solid. Yield: 78 mg (32%). 1H-NMR: 8.58 (s, 1H), 8.38 (d, J=8 Hz, 1H), 8.02 (d, J=8.0 Hz, 1H), 7.82 (s, 1H), 7.77-7.65 (m, 3H), 7.53 (d, J=8.5 Hz, 1H), 7.30 (dd, J=8.5, 1.0 Hz, 1H), 7.22 (t, J=8.0 Hz, 1H), 7.16 (d, J=7.0 Hz, 1H), 6.99 (dt, J=7.5, 7.5, 1.0 Hz, 1H), 4.02 (t, J=8.5 Hz, 2H), 2.92 (t, J=8.5 Hz, 2H), 2.43 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901306B2
Source datasetuspto-grants-2014_12
ORD IDord-a48bc5ddbf5d46a48250ae9ca89e31c5
Source noteuspto-grants-2014_12