Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | HCID 86689154 | HCID 86689154 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86689153 | HCID 86689153 | 93% |
Reaction Steps
To a solution of (R)-4-(6-bromo-3-fluoro-pyridin-2-yl)-5,5-difluoro-4-(2-methoxy-ethyl)-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (200 mg, 0.543 mmol) and triethylamine (110 mg, 1.087 mmol) in dichloromethane (5.4 ml) was added solid 4,4′-dimethoxytrityl chloride (202 mg, 0.598 mmol) under argon atmosphere. The green solution was stirred at rt for 16 hrs and was then evaporated in vacuo. The crude product was taken up with ethyl acetate and washed with aqueous citric acid, aqueous sodium bicarbonate solution, water and brine. The organic phase was dried over sodium sulfate, filtered and evaporated. The crude product (380 mg) was chromatographed over silica gel (Redisep column 12 g, cyclohexane/ethyl acetate 8:2) to give the title compound as a colourless foam. 339 mg (93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09163011B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-1eebde6678a6452dbfaa24c177ce3e18 |
|---|
| Source note | uspto-grants-2015_10 |
|---|