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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511454Generated: October 26, 2026

Acetic Acid → (3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate

https://huagongshe.com/reaction/1511454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl AcetateHCID 8857—
ReactantIsocyanocyclopropaneHCID 2758008—
Reactant(S)-tert-butyl 1-cyclobutyl-3-oxopropan-2-ylcarbamateHCID 57893126—
SolventDichloromethaneHCID 6344—
Product(3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetateHCID 57893114—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of cyclopropylisonitrile (1.21 g, 18 mmol), (S)-tert-butyl 1-cyclobutyl-3-oxopropan-2-ylcarbamate (2.95 g, 13 mmol) in methylene chloride(20 mL), was added acetic acid (1.56 g, 26 mmol) at 0° C. After the addition was complete, the reaction mixture was allowed to warm to 25° C. and stirred for another 4 hours. The reaction mixture was diluted with 200 mL ethyl acetate and washed with a saturated solution of sodium bicarbonate, then brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the crude product was crystallized from 50 mL of ethyl acetate and hexane (v/v=1/1) to give (3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate (3.8 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211897B2
Source datasetuspto-grants-2012_07
ORD IDord-fb0f9205ee744d33ba0aa35a4009f1d5
Source noteuspto-grants-2012_07