HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-6-methoxybenzothiazole → HCID 46912956, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-6-methoxybenzothiazole | HCID 15630 | — |
| Reactant | HCID 66762693 | HCID 66762693 | — |
| Product | HCID 46912956 | HCID 46912956 | — |
Reaction Steps
4-(N-(4-methoxyphenyl)-N-methylsulfamoyl)benzoic acid (7) (100 mg, 0.31 mmol) was treated with 6-methoxybenzo[d]thiazol-2-amine (47 mg, 0.26 mmol) using method C. The residue was purified using flash chromatography eluting with 0-40% EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give N-(6-methoxybenzo[d]thiazol-2-yl)-4-(N-(4-methoxyphenyl)-N-methylsulfamoyl)benzamide as a yellow solid. Yield: 26 mg (21%). 1H-NMR: 8.28 (d, J=8.5 Hz, 2H), 7.74-7.61 (m, 4H), 7.08 (dd, J=9.0, 2.5 Hz, 1H), 7.00 (d, J=8.5 Hz, 2H), 6.91-6.88 (m, 2H), 3.83 (s, 3H), 3.74 (s, 3H), 3.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09416101B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-c0010f5d0e164d67a2486c9aa96bc644 |
| Source note | uspto-grants-2016_08 |