Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264831Generated: October 31, 2026

Methyl (2S)-2-amino-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-4-pentynoate → Methyl (2S)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-3,4-dihydro-2H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/2264831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (2S)-2-amino-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-4-pentynoateHCID 59596690—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
SolventAcetonitrileHCID 6342—
ProductMethyl (2S)-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-3,4-dihydro-2H-pyrrole-2-carboxylateHCID 59596699100.4%

Reaction Steps

To a solution of methyl (2S)-2-amino-5-(5-{[(2-fluorophenyl)methyl]oxy}-2-pyridinyl)-4-pentynoate (D84, 300 mg, 0.91 mmol) in acetonitrile was added silver triflate (24 mg, 0.091 mmol) and the mixture was stirred for 60 hours at room temperature. The solvent was evaporated and the residue diluted with water and extracted with ethyl acetate. The organic layer was dried (Na2SO4), filtered and evaporated affording the title compound as a yellow solid (300 mg, quantitative). Rt (HPLC): 3.58 min; MS: (ES/+) m/z: 329 [MH]+ C18H17FN2O3 requires 328.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855218B2
Source datasetuspto-grants-2010_12
ORD IDord-15b89085943d44daa82387a4214e9ab0
Source noteuspto-grants-2010_12