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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387471Generated: November 1, 2026

Sodium borohydride → HCID 86601776, compound

https://huagongshe.com/reaction/2387471

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 numberUS08268826B2
Source datasetuspto-grants-2012_09
ORD IDord-337d3ce7830b404a8748d266201486a3
Source noteuspto-grants-2012_09