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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-6-methylbenzothiazole | HCID 17335 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(2,3-dihydro-1H-indole-1-sulfonyl)benzoic acid | HCID 3807505 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(indolin-1-ylsulfonyl)-N-(6-methylbenzo[d]thiazol-2-yl)benzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901306B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a48bc5ddbf5d46a48250ae9ca89e31c5 |
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| Source note | uspto-grants-2014_12 |
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