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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178794Generated: October 30, 2026

Sodium borohydride → HCID 86601776, compound

https://huagongshe.com/reaction/2178794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68743987HCID 68743987—
SolventEthanolHCID 702—
ProductHCID 86601776HCID 86601776—

Reaction Steps

To a solution of tert-butyl 4-methyl-4-{3-methyl-4-[3-oxo-5-(trifluoromethyl)-2,3-dihydro-1H-inden-1-yl]piperazin-1-yl}piperidine-1-carboxylate (100 mg, 0.202 mmol) in ethanol (7 mL) was added sodium borohydride (57 mg, 1.5 mmol). The reaction mixture was stirred at room temperature for 2 h. The solvent was evaporated in vacuo, and the residue was quenched with 10 mL of 1 N aqueous NaOH solution and 10 mL of EtOAc. The organic phase was separated and the aqueous layer was extracted with EtOAc twice (2×15 mL). The combined extracts were washed with brine, dried over Na2SO4 and evaporated under reduced pressure to give the desired product which was directly used for the next step (93 mg, 92%). LC-MS [M+1]=498.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067921B2
Source datasetuspto-grants-2015_06
ORD IDord-4b6609cb2b02471284aa92978cc13f6f
Source noteuspto-grants-2015_06