HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → (7-Bromo-5-methyl-2,3-dihydrobenzo[b]oxepin-4-yl)methyl carbamimidothioate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 7-Bromo-4-(chloromethyl)-5-methyl-2,3-dihydrobenzo[b]oxepine | HCID 86685422 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (7-Bromo-5-methyl-2,3-dihydrobenzo[b]oxepin-4-yl)methyl carbamimidothioate hydrochloride | HCID 86685423 | 102% |
Reaction Steps
To a solution of 7-bromo-4-(chloromethyl)-5-methyl-2,3-dihydrobenzo[b]oxepine from step H7 (2.05 g, 7.13 mmol) in ethanol (75 mL) was added thiourea (0.651 g, 8.55 mmol). The mixture was refluxed for 3 h. A white solid precipitated. The solvent was removed. The solid residue was washed with hexanes and dried in vacuo to give a (7-bromo-5-methyl-2,3-dihydrobenzo[b]oxepin-4-yl)methyl carbamimidothioate hydrochloride (2.64 g, 7.26 mmol, 102% yield). The crude mixture was used in the next step without further purification. 1H NMR (500 MHz, methanol-d4) δ 7.48 (d, J=2.4 Hz, 1H), 7.43-7.36 (m, 1H), 6.97 (d, J=8.5 Hz, 1H), 4.53 (t, J=6.3 Hz, 2H), 4.25 (s, 2H), 2.34 (t, J=6.1 Hz, 2H), 2.18 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604024B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-e1d3a453be67490db58cf8b300b35619 |
| Source note | uspto-grants-2013_12 |