HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(4aR,6R,8aS)-6-[(benzyloxy)methyl]-8a-(2,4-difluorophenyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide → HCID 90253541, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(4aR,6R,8aS)-6-[(benzyloxy)methyl]-8a-(2,4-difluorophenyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide | HCID 86729526 | — |
| Reactant | HCID 90253548 | HCID 90253548 | — |
| Product | HCID 90253541 | HCID 90253541 | — |
Reaction Steps
N-({(3S,4R,6R)-3-(2,4-Difluorophenyl)-4-(hydroxymethyl)-6-[(2S)-tetrahydrofuran-2-yl]tetrahydro-2H-pyran-3-yl}carbamothioyl)benzamide (C102) was converted to the product using the method described for the synthesis of N-[(4aR,6R,8aS)-6-[(benzyloxy)methyl]-8a-(2,4-difluorophenyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide (C8) in Preparation P1. Yield: 1.0 g, 2.2 mmol, 87%. LCMS m/z 458.9 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403846B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-5674aaa42edd454285e149c7b72cbc9c |
| Source note | uspto-grants-2016_08 |