HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473846Generated: October 30, 2026
HCID 49833869, compound → HCID 49833692, compound
https://huagongshe.com/reaction/473846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 49833869 | HCID 49833869 | — |
| Solvent | Ethanol, mixt. with methanol | HCID 18681192 | — |
| Product | HCID 49833692 | HCID 49833692 | — |
Reaction Steps
Prepared by chiral preparative HPLC separation of racemic 7-(2-methyl-1H-benzimidazol-6-yl)-4-[(2-phenylpiperidin-1-yl)carbonyl]-2,3,4,5-tetrahydro-1,4-benzoxazepine (example 1) using a SHIMADZU LC-20AD apparatus equipped with a Chiralpak AD-H, 25 cm×4.6 mm column using a mobile phase of ethanol:methanol 1:1 and flow rate of 18.0 mL/min and detection at 220 nm. The isomer with retention time 11.20 min. was assigned as the (R)-enantiomer. Chiral analytical HPLC was carried out using a SHIMADZU LC-20AD apparatus equipped with a Chiralpak AD-H, 25 cm×4.6 mm column using a mobile phase of ethanol:methanol 1:1 and flow rate of 0.7 mL/min with detection at 254/220 nm. This isomer gave a retention time 9.51 min and ee>99%. MS (EI) C29H30N4O2: 467 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637499B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-57957190658e4b5c97ba802612a654eb |
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| Source note | uspto-grants-2014_01 |
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