HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472722Generated: October 30, 2026
Lithium borohydride → HCID 58169903, compound
https://huagongshe.com/reaction/472722
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 58169887 | HCID 58169887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58169903 | HCID 58169903 | 47.9% |
Reaction Steps
To a solution of methyl (2R,5S,7R)-8-{[{(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethyl}(methyl)amino]carbonyl}-7-(4-fluoro-2-methylphenyl)-1,8-diazaspiro[4.5]decane-2-carboxylate (Intermediate 12, 350 mg, 0.580 mmol) in Tetrahydrofuran (THF) (6 ml) at 0° C. lithium borohydride (0.568 ml, 1.160 mmol) was added and the reaction mixture was stirred at room temperature and under nitrogen atmosphere overnight. Volatiles were evaporated in vacuo and the residue was dissolved in Methanol (2 ml)/HCl 1 N in water (4 ml). After 1 h stirring combined solvents were evaporated in vacuo. The residue was dissolved in Ethyl acetate (4 ml) and washed with NaHCO3 sat. sol. (2×3 ml). Organic phase was dried and evaporated and the residue was purified by flash chromatography on silica gel using a Biotage 12+M as column and Dichloromethane/Methanol 95:5 as eluent affording the title compound (160 mg, 0.278 mmol, y=47.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633214B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-36c7ae0596864a429acc195e88883326 |
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| Source note | uspto-grants-2014_01 |
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