HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350211Generated: October 30, 2026
HCID 60077679, compound → HCID 60077668, compound
https://huagongshe.com/reaction/1350211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 60077679 | HCID 60077679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 60077668 | HCID 60077668 | 73.3% |
Reaction Steps
A solution of tert-butyl(3R)-3-[3-(1-benzhydryl-3-azetidinyl)-1,2,4-oxadiazol-5-yl]-6-cyclohexylhexanoate (preparation 36) (1.99 g, 3.66 mmol) in DCM (15 ml) was treated with ACE-CI (530 μl, 4.90 mmol) and heated at reflux for 4 hours. The solvent was removed under reduced pressure. The residue was dissolved in MeOH (15 ml) and heated at reflux for 1.5 hours. The solvent was removed under reduced pressure. The oil was dissolved in EtOAc (150 ml) and washed with sat. NaHCO3 solution (50 ml) and brine (40 ml). The aqueous extracts were combined and extracted with EtOAc. All of the organic extracts were combined, dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure to afford the title compound as a colourless oil (900 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07214694B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-edd9ffa13ea34c3cb9aa69d865e61fa8 |
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| Source note | uspto-grants-2007_05 |
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