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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384044Generated: October 30, 2026

Lithium borohydride → HCID 58169912, compound

https://huagongshe.com/reaction/384044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 58169926HCID 58169926—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58169912HCID 5816991266.8%

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)-2-methyl-1,8-diazaspiro[4.5]decane-2-carboxylate (Intermediate 44, 69 mg, 0.112 mmol) in Tetrahydrofuran (THF) (2.5 ml) at 0° C. lithium borohydride (0.164 ml, 0.335 mmol) was added and the reaction mixture was stirred at room temperature and under nitrogen atmosphere for 3 days. Volatiles were evaporated in vacuo and the residue was dissolved in Methanol (2 ml)/HCl 1 N in water (3 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 SNAP 10 g as column and Dichloromethane/Methanol 95:5 as eluent affording the title compound (28 mg, 0.047 mmol, y=66.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367692B2
Source datasetuspto-grants-2013_02
ORD IDord-38b488ec7c5d416088fdb9ba25b92c2c
Source noteuspto-grants-2013_02