HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-Hydroxy-2-methylpropan-2-yl)thiourea → 2-(8-Bromo-4,5-dihydrothiazolo[4,5-d]benzo[b]oxepine-2-ylamino)-2-methylpropan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-Hydroxy-2-methylpropan-2-yl)thiourea | HCID 22768414 | — |
| Reactant | 4,8-dibromo-3,4-dihydrobenzo[b]oxepin-5(2H)-one | HCID 57900275 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(8-Bromo-4,5-dihydrothiazolo[4,5-d]benzo[b]oxepine-2-ylamino)-2-methylpropan-1-ol | HCID 58204262 | — |
Reaction Steps
A mixture of 0.67 g (5.0 mmol) of 1-(1-hydroxy-2-methylpropan-2-yl)thiourea and 1.60 g (5.00 mmol) of 4,8-dibromo-3,4-dihydro-2Hbenzo[b]oxepin-5-one in 30 ml of ethanol was heated under reflux for 3 hours. The mixture was concentrated, the residue purified on silica gel column eluting the product with 10% of methanol in dichloromethane. Yield 1.38 g (75%). MS(ESI+): 369.3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09175009B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-93d8730cbb8345499cb59e46d93e85cd |
| Source note | uspto-grants-2015_11 |