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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898647Generated: November 1, 2026

Hydrochloric Acid → HCID 67385839, compound

https://huagongshe.com/reaction/1898647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(R)-2-((tert-Butoxycarbonyl)amino)-2-cyclopropylacetic acidHCID 7146275—
ReactantAzetidine-3-carbonitrile hydrochlorideHCID 45072465—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67385839HCID 6738583983.5%

Reaction Steps

(R)-2-(tert-butoxycarbonylamino)-2-cyclopropylacetic acid (2.25 g, 10.5 mmol) and O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium tetrafluoroborate (3.69 g, 11.5 mmol) were dissolved in dichloromethane (105 mL). 3-Cyanoazetidine hydrochloride (1.36 g, 11.5 mmol) and then N,N-diisopropylethylamine (4.5 mL, 26.1 mmol) were added and the mixture was stirred at room temperature for 5 h. Water, dilute HCl and more dichloromethane were added, the layers were separated and the aqueous layer was extracted once more with dichloromethane. The combined organic layers were washed with sodium chloride solution, dried over sodium sulfate and concentrated. The residue was purified by silica gel chromatography (methanol/dichloromethane) to give 2.45 g (83%) of [(R)-2-(3-cyano-azetidin-1-yl)-1-cyclopropyl-2-oxo-ethyl]-carbamic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518945B2
Source datasetuspto-grants-2013_08
ORD IDord-0bd8351d38d6410ea14c90a426e600a6
Source noteuspto-grants-2013_08