HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656347Generated: October 28, 2026
Water → (3S)-N-(7-oxoazepan-4-yl)-1-phenylpiperidine-3-carboxamide
https://huagongshe.com/reaction/656347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | (3S)-N-(4-oxocyclohexyl)-1-phenylpiperidine-3-carboxamide | HCID 11688042 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (3S)-N-(7-oxoazepan-4-yl)-1-phenylpiperidine-3-carboxamide | HCID 11638247 | — |
Reaction Steps
To a solution of (3S)-N-(4-oxocyclohexyl)-1-phenylpiperidine-3-carboxamide (10 mg, 0.00003 mol, prepared as example 171) in concentrated aqueous HCl (0.5 mL), was added sodium azide (2.27 mg, 0.0000350 mol) in small portions over 3 minutes with slow agitation. The temperature was slowly increased to 50° C. The reaction temperature was maintained at 50° C. for 8.5 h and then poured into 50 g of crushed ice and water. The solution was basified with cold 50% NaOH and the resulting solution was extracted with EtOAc(×3). The EtOAc extracts were combined, dried over MgSO4, filtered and evaporated to yield the crude product, which was purified by prep-HPLC. LCMS: (M+H)+=316.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071624B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2469ec55cb51436e9a4327f2865a2cab |
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| Source note | uspto-grants-2011_12 |
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