HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 58691359, compound → HCID 58691309, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 58691359 | HCID 58691359 | — |
| Reactant | HCID 58691392 | HCID 58691392 | — |
| Product | HCID 58691309 | HCID 58691309 | — |
Reaction Steps
(2R)-N-(2-(6-(2-Acetamidobenzo[d]thiazol-4-yloxy)pyrimidin-4-yl)-5-(trifluoromethyl)phenyl)-1-isobutylpiperidine-2-carboxamide and (2S)-N-(2-(6-(2-Acetamidobenzo[d]thiazol-4-yloxy)pyrimidin-4-yl)-5-(trifluoromethyl)phenyl)-1-isobutylpiperidine-2-carboxamide. Chiral separation [Chiralcel OD-H (250×21 mm, 5μ), A: hexane (0.2% diethylamine), B: ethanol (0.2% diethylamine), isocratic: 60:40 A:B, 20 mL/min] of N-(2-(6-(2-acetamidobenzo[d]-thiazole-4-yloxy)pyrimidin-4-yl)-5-(trifluoromethyl)phenyl)-1-isobutylpiperidine-2-carboxamide (Example 51) afforded the title compounds as amorphous solids. MS (ESI, pos. ion) m/z: 613 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07301022B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-87ea432abaa24f599970c9c2e1a11888 |
| Source note | uspto-grants-2007_11 |