HuagongsheHuagongshe Chemistry Print Report · For research reference only
(5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanol → HCID 69595763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanol | HCID 2776149 | — |
| Reactant | 3,5-Difluoro-4-(hydroxymethyl)phenol | HCID 22219975 | — |
| Reactant | rel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylate | HCID 86585999 | — |
| Product | HCID 69595763 | HCID 69595763 | — |
Reaction Steps
cis-2,6-Dimethyl-piperazine-1-carboxylic acid 2,6-difluoro-4-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-benzyl ester was prepared from 2,6-difluoro-4-hydroxybenzyl alcohol, (5-methyl-3-phenyl-isoxazol-4-yl)-methanol and 1-chlorocarbonyl-cis-2,6-dimethyl-4-tert-butoxycarbonylpiperazine according to the procedures described for Example 54 and 121 to give the product as a yellow oil: δH (400 MHz; d6-DMSO) 1.15 (6H, d, J 7.0 Hz), 2.53 (3H, s), 2.62 (2H, dd, J 12.0, 4.5 Hz), 2.68 (2H, d, J 12.0 Hz), 3.80–3.88 (2H, m), 5.01–5.08 (4H, m), 6.84–6.91 (2H, m), 7.48–7.53 (3H, m) and 7.64–7.68 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022707B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-4ff256885a5149308af15242f4dcf20f |
| Source note | uspto-grants-2006_04 |