HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Diacetyl-O-methylhydroxylamine → HCID 58909414, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Diacetyl-O-methylhydroxylamine | HCID 538412 | — |
| Reactant | HCID 58909477 | HCID 58909477 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58909414 | HCID 58909414 | 99% |
Reaction Steps
To a solution of benzyl 4-{[(2R,3S)-3-amino-4-(3,5-difluorophenyl)-2-hydroxybutyl]amino}-6-neopentyl-3,4-dihydroquinoline-1(2H)-carboxylate (0.226 g) in dichloromethane (5 mL) was added N,N-diacetyl-O-methylhydroxylamine (0.064 9). The mixture was stirred over the weekend at room temperature. The solvent was then removed under reduced pressure and the residue was partitioned between 1N HCl and ethyl acetate, dried with magnesium sulfate, filtered, and concentrated to give 0.243 g of the title compound. (99% yield). MS (ESI+) for C34H41F2N3O4 m/z 594.31 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244725B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-453e6f34423a44cfb6057188e2c4c194 |
| Source note | uspto-grants-2007_07 |