HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylthiourea → 2-Methylamino-5,6-dihydro-4H-benzothiazol-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | 2-Bromocyclohexane-1,3-dione | HCID 2770476 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Methylamino-5,6-dihydro-4H-benzothiazol-7-one | HCID 3427490 | 43% |
Reaction Steps
A solution of 2-bromo-cyclohexane-1,3-dione (8.0 g, 41.9 mmol) and methyl thiourea (3.77 g, 41.9 mmol) in pyridine (63 mL) was stirred at room temperature for 16 h. The reaction mixture was concentrated under vacuum, extracted with CH2Cl2 /10% aq NaCl solution, dried, filtered, and concentrated under vacuum. Crystallization from EtOAc afforded the title compound as yellow crystals (3.26 g, 43%): mp 180-182° C. Anal. RP-HPLC: tR 8.4 min (0-60% MeCN, purity 100%). 1H-NMR (CDCl3): δ 7.90 (s, 1H, NH), 2.99 (s, 3H, CH3), 2.72 (t, 2H, J 6.1, CH2), 2.49 (t, 2H, J 6.1, CH2), 2.10 (qu, 2H, J 6.1, CH2). 13C-NMR (CDCl3): δ 191.0, 176.6, 168.0, 120.0, 37.5, 32.5, 27.7, 23.2. MS: (ESI+) m/z 183.07 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576091B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-3a878cd7311a4754a19f1aa0345b618a |
| Source note | uspto-grants-2009_08 |