HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24804395, compound → N-Methyl-2-(6-methylaminopyridin-3-yl)benzothiazol-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24804395 | HCID 24804395 | — |
| Reactant | tert-Butyl (5-{6-[(tert-butoxycarbonyl)(methyl)amino]-1,3-benzothiazol-2-yl}pyridin-2-yl)methylcarbamate | HCID 86626545 | — |
| Product | N-Methyl-2-(6-methylaminopyridin-3-yl)benzothiazol-6-amine | HCID 24804556 | — |
Reaction Steps
tert-Butyl (5-{6-[(tert-butoxycarbonyl)(methyl)amino]-1,3-benzothiazol-2-yl}pyridin-2-yl)methylcarbamate (53 mg, 0.11 mmol) was reacted according to the procedure used for the preparation of 2-(6-methylaminopyridin-3-yl)benzothiazol-6-amine. This gave the title compound (20 mg) as a yellow solid. 1H NMR δ 8.56 (d, 1H) 7.91 (dd, 1H) 7.63 (d, 1H) 7.12 (br q, 1H) 7.00 (d, 1H) 6.75 (dd, 1H) 6.55 (d, 1H) 5.99 (br q, 1H) 2.84 (d, 3H) 2.73 (d, 3H); MS m/z (M+H) 271.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163928B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-785a7783528945ffa0b1e1073e307f67 |
| Source note | uspto-grants-2012_04 |