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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429152Generated: October 30, 2026

Hydrochloric Acid → 1-[(3-Oxo-2-oxa-bicyclo[2.2.1]heptane-5-carbonyl)-amino]-2-vinyl-cyclo-propane carboxylic acid ethyl ester

https://huagongshe.com/reaction/1429152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
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—
ReactantEthyl 1-amino-2-vinylcyclopropanecarboxylateHCID 22082824—
Reactant3-Oxo-2-oxabicyclo[2.2.1]heptane-5-carboxylic acidHCID 46244965—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-[(3-Oxo-2-oxa-bicyclo[2.2.1]heptane-5-carbonyl)-amino]-2-vinyl-cyclo-propane carboxylic acid ethyl esterHCID 6687043499%

Reaction Steps

To a solution of compound 3b (857 mg, 5.5 mmol), in DMF (14 mL) and DCM (25 mL) at room temperature, was added the hydrochloride of 1-amino-2-vinyl-cyclopropanecarboxylic acid ethyl ester, prepared as described in WO03/099274, (1.15 g, 6.0 mmol), HATU (2.29 g, 6.0 mmol) and DIPEA (3.82 mL, 22 mmol). The reaction was stirred under N2-atmosphere at ambient temperature for 1 h. LC/MS analysis showed complete conversion and the reaction mixture was concentrated in vacuo. The residue was redissolved in DCM (100 ml) and 0.1 M HCl (aq) and the phases were separated. The organic phase was washed with NaHCO3 (aq) and brine, dried (MgSO4) and filtered. Removal of the solvent in vacuo afforded the target compound (1.6 g, 99%). LC/MS >95%, m/z (ESI+)=294 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937080B2
Source datasetuspto-grants-2015_01
ORD IDord-46a00263fddc4db98f02531c98777395
Source noteuspto-grants-2015_01