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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912432Generated: October 30, 2026

Diisopropylethylamine → 6-Benzyl-3-methyl-1,6-diazaspiro[3.4]octan-5-one

https://huagongshe.com/reaction/1912432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant[Benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl esterHCID 58293285—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product6-Benzyl-3-methyl-1,6-diazaspiro[3.4]octan-5-oneHCID 58293310—

Reaction Steps

To a solution of an optically-active compound of 2-(2-benzylaminoethyl)-3-methylazetidine-2-dicarboxylic acid 2 hydrochloride (29.1 g) and N,N-diisopropylethylamine (65 ml) in chloroform (290 ml) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (41.3 g) at room temperature, and the mixture was stirred for 4 hours. To the reaction mixture were added saturated aqueous sodium bicarbonate solution (200 ml) and water (100 ml), and the mixture was extracted with chloroform (200 ml). The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: chloroform/methanol=20/1 to 10/1) to give the titled compound (21.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-ddf6417373e94bbea796931eafa0421d
Source noteuspto-grants-2013_12