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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689271Generated: October 30, 2026

Methanol → 2-(Diphenylmethyl)-5-oxa-2,8-diazaspiro[3.5]nonane

https://huagongshe.com/reaction/1689271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant2-Benzhydryl-5-oxa-2,8-diazaspiro[3.5]nonan-7-oneHCID 57989264—
SolventTetrahydrofuranHCID 8028—
Product2-(Diphenylmethyl)-5-oxa-2,8-diazaspiro[3.5]nonaneHCID 57989237—

Reaction Steps

Borane methyl sulfide complex (2M in THF, 10.7 mL) was added to a solution of 2-benzhydryl-5-oxa-2,8-diazaspiro[3.5]nonan-7-one (example 33, step e) (2 g) in dry THF (40 mL) and the resultant solution was stirred at 70° C. under nitrogen for 50 minutes. The mixture was cooled to room temperature and treated dropwise with methanol (40 mL) followed by N1,N2-dimethylethane-1,2-diamine (3.43 g). The mixture was heated at 70° C. for 6 hours. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and brine. The organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 1% triethylamine and 5% methanol in dichloromethane as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 1.35 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-3ec69db7bfa74476b03033f4afc05426
Source noteuspto-grants-2012_04