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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171956Generated: October 25, 2026

Diisopropylethylamine → (1R,2S)-ethyl 1-((2S,4R)-1-((5)-4-(but-enyloxy)-2-(tert-butoxycarbonylamino)butanoyl)-4-hydroxypyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylate

https://huagongshe.com/reaction/1171956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant(S)-4-(but-3-enyloxy)-2-(tert-butoxycarbonylamino)-butanoic acidHCID 59554212—
Reactant(1R,2S)-ethyl 1-((3R,5S)-3-hydroxypyrrolidine-5-carboxamido)-2-vinylcyclopropanecarboxylate hydrochlorideHCID 67330424—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(1R,2S)-ethyl 1-((2S,4R)-1-((5)-4-(but-enyloxy)-2-(tert-butoxycarbonylamino)butanoyl)-4-hydroxypyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylateHCID 86611242—

Reaction Steps

(1R,2S)-ethyl-1-((2S,4R)-4-hydroxypyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylate hydrochloride salt (WO2005095403) (1.21 g, 3.84 mmol), (S)-4-(but-3-enyloxy)-2-(tert-butoxycarbonylamino)-butanoic acid (1.00 g, 3.66 mmol) and HATU (1.53 g, 4.03 mmol) in toluene (18 mL) and ACN (2 mL) was added DIEA (1.28 mL, 4.03 mmol) at 0° C. The reaction warmed to rt and stirred at rt for 1 hr. Ethyl acetate (30 mL) and water (20 mL) was added. The organic layer was separated and washed with brine, dried over sodium sulfate. After removal of solvent, the residue was purified by chromatography (Ethyl acetate) to give (1R,2S)-ethyl 1-((2S,4R)-1-((S)-4-(but-enyloxy)-2-(tert-butoxycarbonylamino)butanoyl)-4-hydroxypyrrolidine-2-carboxamido)-2-vinylcyclopropanecarboxylate as white wax solid (1.7 g, 89%). MS: Calcd.: 523; Found: [M+H]+ 524.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829665B2
Source datasetuspto-grants-2010_11
ORD IDord-b877a5975f9445c2be8c9e17c7b848ca
Source noteuspto-grants-2010_11