HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 6-Methoxybenzothiazole | HCID 350186 | — |
| Reactant | 5-Bromopyridine-2-carboxamide | HCID 735151 | — |
| Reactant | 6-Methoxy-2-[5-(trifluoromethyl)pyridin-2-yl]-1,3-benzothiazole | HCID 24803891 | — |
| Catalyst | Bis(tri-tert-butylphosphine)palladium(0) | HCID 2734558 | — |
| Product | 5-(5-methoxy-1,3-benzothiazol-2-yl)-N-methylpyridin-2-amine | HCID 24803727 | — |
Reaction Steps
6-Methoxy-1,3-benzothiazole (0.100 g, 0.61 mmol) and 5-bromopyridine-2-carboxamide (0.146 g, 0.73 mmol) were reacted according to the procedure used for the preparation of 6-methoxy-2-[5-(trifluoromethyl)pyridin-2-yl]-1,3-benzothiazole, with the following exceptions: 10 mol % bis(tri-t-butylphosphine) palladium (0) was used and the amount of DMF was reduced (3 mL). The reaction mixture was concentrated and flash chromatography of the residue gave the title compound (10 mg) as an off-white solid. 1H NMR δ 9.25 (dd, 1H) 8.56 (dd, 1H) 8.23 (br s, 1H) 8.19 (dd, 1H) 8.04 (d, 1H) 7.81 (d, 1H) 7.78 (br s, 1H) 7.20 (dd, 1H) 3.88 (s, 3H); MS m/z (M+H) 286.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163928B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-0a7af11e834c44c9b2aaeca42eb564ce |
| Source note | uspto-grants-2012_04 |