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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482845Generated: October 31, 2026

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

https://huagongshe.com/reaction/1482845

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 numberUS09416101B2
Source datasetuspto-grants-2016_08
ORD IDord-a62e8173307e4485bd31c05a97af143a
Source noteuspto-grants-2016_08