HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57432117, compound → HCID 16122905, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57432117 | HCID 57432117 | — |
| Reactant | HCID 57432118 | HCID 57432118 | — |
| Product | HCID 16122905 | HCID 16122905 | — |
Reaction Steps
(S)-(+)-4-benzyl-N-(3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-N-isobutylmorpholine-2-carboxamide and (R)-(−)-4-benzyl-N-(3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-N-isobutylmorpholine-2-carboxamide. Resolution into the pure enantiomers was performed by preparative HPLC using isocratic elution on ChiralPak AD at 1 mL/min, eluting with 100% ethanol. Under these conditions, the (R)-(−)-isomer elutes second after the (S)-(+)-isomer. (S)-(+)-4-benzyl-N-(3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-N-isobutylmorpholine-2-carboxamide: [α]D25° C.=+10° (c=1, MeOH), (R)-(−)-4-benzyl-N-(3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-N-isobutylmorpholine-2-carboxamide: [α]D25° C.=−10° (c=1, MeOH)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855201B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-f0dcb4d66c454b91bb2e29ca4b05fa58 |
| Source note | uspto-grants-2010_12 |