HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12795Generated: October 29, 2026
Sodium Hydroxide → HCID 86615961, compound
https://huagongshe.com/reaction/12795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 58994175 | HCID 58994175 | — |
| Reactant | (1S,5R)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane | HCID 59337591 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86615961 | HCID 86615961 | 16% |
Reaction Steps
3-[5-(3-Fluoro-pyridin-4-yl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-propionaldehyde (Prep69, 63 mg, 0.24 mmol) was dissolved in DCM-MeOH 1-1 (2 ml). The resulting solution was cooled at 0° C. and then (1S,5R)-1-(4-trifluoromethyl-phenyl)-3-aza-bicyclo[3.1.0]hexane (54 mg, 0.24 mmol), AcOH (17 μl) and NaBH(AcO)3 (55 mg, 0.26 mmol) were added. The mixture was left to reach room temperature and the stirring was prolonged for further 18 hours. 1N NaOH was added and the product was extracted with DCM. The organic phase was dried (Na2SO4) and evaporated. The crude was redissolved in DCM and treated with PS-isocyanate (300 mg) overnight. The residue was finally purified with SCX cartridge, washing with MeOH and then collecting the product with MeOH—NH4OH (95-5) to give 17 mg of the title compound (16% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727988B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-a63941edc6754ed2b147e6f104c0245a |
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| Source note | uspto-grants-2010_06 |
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