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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727725Generated: October 31, 2026

Diisopropylethylamine → HCID 86752013, compound

https://huagongshe.com/reaction/727725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantAzetidin-3-amine--hydrogen chloride (1/2)HCID 13491919—
ReactantHCID 15297072HCID 15297072—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 86752013HCID 86752013—

Reaction Conditions

Temperature40 °C

Reaction Steps

1.62 g of (2S,4S)-4-(4-methoxybenzylthio)-1-methyl-2-pyrrolidinecarboxylic acid were suspended in 20 ml of dry acetonitrile, and 1.02 g of N,N'-carbonyldiimidazole were added to the suspension, after which the mixture was stirred at 40° C. for 45 minutes. A solution of 1.00 g of 3-aminoazetidine dihydrochloride and 2.40 ml of diisopropylethylamine in 10 ml of methanol was added dropwise to the mixture, whilst ice-cooling, and the mixture was stirred at the same temperature for 90 minutes. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure. The resulting residue was subjected to reverse phase column chromatography (Cosmosil 75C18 -PREP, manufactured by Nacalai Tesque, 145 g) to give 1.21 g of the title compound, as a colorless oil, from the fraction obtained by solution with 30% by volume aqueous acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712267
Source datasetuspto-grants-1998_01
ORD IDord-b7e0bcf4ea764c05a5d92bba3bd299ac
Source noteuspto-grants-1998_01