HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzothiazol-5-amine → 5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzothiazol-5-amine | HCID 70749 | — |
| Reactant | 5-Bromo-N-methylpyridin-2-amine | HCID 15645663 | — |
| Reactant | 2-(2-Methoxypyrimidin-5-yl)-1,3-benzothiazole | HCID 24803726 | — |
| Product | 5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amine | HCID 24803727 | — |
Reaction Steps
The title compound was prepared according to the method used for the preparation of 2-(2-methoxypyrimidin-5-yl)-1,3-benzothiazole, now starting from 1,3-benzothiazol-5-amine (50 mg, 0.33 mmol) and 5-bromo-N-methylpyridin-2-amine (75 mg, 0.40 mmol). The crude material was purified on a preparative HPLC to give the title compound (12 mg) as a pale beige solid. 1H NMR δ ppm 8.62 (d, 1 H) 7.95 (dd, 1 H) 7.61 (d, 1 H) 7.19 (q, 1 H) 7.07 (d, 1 H) 6.69 (dd, 1 H) 6.56 (d, 1 H) 5.24 (s, 2 H) 2.85 (d, 3 H); MS m/z (M+H) 257.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957215B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-28769d567c3344cf858f94a9f1481b1b |
| Source note | uspto-grants-2015_02 |