Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190018Generated: November 2, 2026

Sodium borohydride → HCID 69812189, compound

https://huagongshe.com/reaction/2190018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68762560HCID 68762560—
SolventMethanolHCID 887—
ProductHCID 69812189HCID 6981218974%

Reaction Steps

To a stirred solution of (R)-tert-butyl 5-(3-fluorobenzoyl)-1-(5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-1′-carboxylate (0.047 g, 0.087 mmol) in MeOH (0.5 mL) was added NaBH4 (0.0036 g, 0.095 mmol) at about 0° C. The reaction was stirred for 1.5 hours and quenched by the addition of saturated NH4Cl solution. The solvent was evaporated under reduced pressure. The solid was dissolved in water and extracted with EtOAc. The combined extracts were washed with brine, dried MgSO4, filtered and concentrated. The crude residue was purified by column chromatography (1-3% MeOH/DCM) to yield tert-butyl 5-((3-fluorophenyl)(hydroxy)methyl)-1-((R)-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[indoline-3,4′-piperidine]-1′-carboxylate (0.035 g, 74%). LCMS (APCI+) m/z 545.3 [M+H]+; Rt=4.02 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324221B2
Source datasetuspto-grants-2012_12
ORD IDord-42fc22e63e81481e80b58f82a82acb93
Source noteuspto-grants-2012_12