HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615796Generated: October 31, 2026
Acetic Acid → (3R)-3-(3,5-Difluorophenyl)-3-methyl-1,4-diazaspiro[5,5]undecan-5-one
https://huagongshe.com/reaction/1615796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 1-{[2-amino-2-(3,5-difluorophenyl)propyl]amino}cyclohexanecarboxylate | HCID 66864381 | — |
| Product | (3R)-3-(3,5-Difluorophenyl)-3-methyl-1,4-diazaspiro[5,5]undecan-5-one | HCID 58118683 | — |
Reaction Steps
A solution of methyl 1-{[2-amino-2-(3,5-difluorophenyl)propyl]amino}cyclohexane carboxylate from Step F (205 mg, 0.628 mmol), and AcOH (0.36 mL, 6.28 mmol) in xylenes (5 mL) was heated at 80° C. for 3 h, allowed to cool, then poured into saturated aqueous NaHCO3 (5 mL). The resulting mixture was extracted with EtOAc (2×10 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of EtOAc:MeOH—100:0 to 92:8, to give the racemic product. The enantiomers were separated by HPLC, using a ChiralPak AD column and eluting with hexane:EtOH:Et2NH—40:60:0.1. The first major peak to elute was (3R)-3-(3,5-difluorophenyl)-3-methyl-1,4-diazaspiro[5.5]undecan-5-one, the title compound, and the second major peak to elute was (3S)-3-(3,5-difluorophenyl)-3-methyl-1,4-diazaspiro[5.5]undecan-5-one. MS: m/z=295 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765759B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-2348223799824bb8ab2a7967e3a2703b |
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| Source note | uspto-grants-2014_07 |
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