HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2,6-difluorobenzoyl)-3-amino-3-(4-chlorophenyl) 1-propanol → 2-(2,6-difluorophenyl)-4-(3-tert-butylphenyl)-5,6-dihydro(4H)1,3-oxazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2,6-difluorobenzoyl)-3-amino-3-(4-chlorophenyl) 1-propanol | HCID 15790732 | — |
| Reactant | N-(2,6-difluorobenzoyl)-3-amino-3-(3-tert-butylphenyl)-1-propanol | HCID 22115246 | — |
| Product | 2-(2,6-difluorophenyl)-4-(3-tert-butylphenyl)-5,6-dihydro(4H)1,3-oxazine | HCID 22115237 | 68.6% |
Reaction Steps
The procedure is as for Example 85, but 4.0 g (11.5 mmol) of N-(2,6-difluorobenzoyl)-3-amino-3-(3-tert-butylphenyl)-1-propanol are employed instead of N-(2,6-difluorobenzoyl)-3-amino-3-(4-chlorophenyl) 1-propanol. 2.6 g (68.6%) of 2-(2,6-difluorophenyl)-4-(3-tert-butylphenyl)-5,6-dihydro(4H)1,3- oxazine are obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166010 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-85699c27bf744c7cbf80c19b5d90ae80 |
| Source note | uspto-grants-2000_12 |