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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600271Generated: October 26, 2026

2-(Tert-butoxycarbonylmethyl-amino)-propionic acid methyl ester → {3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-5-methyl-2,4-dioxo-imidazolidin-1-yl}-acetic acid tert-butyl ester

https://huagongshe.com/reaction/600271

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tert-butoxycarbonylmethyl-amino)-propionic acid methyl esterHCID 21643734—
Reactant4-(4-Fluoro-3-isocyanato-benzyl)-2H-phthalazin-1-oneHCID 59856545—
SolventDichloromethaneHCID 6344—
Product{3-[2-Fluoro-5-(4-oxo-3,4-dihydro-phthalazin-1-ylmethyl)-phenyl]-5-methyl-2,4-dioxo-imidazolidin-1-yl}-acetic acid tert-butyl esterHCID 68910449—

Reaction Steps

To a suspension of 4-(3-isocyanato-benzyl)-2H-phthalazin-1-one (2)(3.12 mmol) in dry DCM (80 ml) in the presence of activated 4 Å molecular sieves (ca 5 g) was added 2-(tert-butoxycarbonylmethyl-amino)-propionic acid methyl ester (33A)(1.07 g, 4.7 mmol). The reaction was then stirred for 48 hours at ambient temperature. HPLC analysis showed there to a mixture of cyclised and uncyclised ureas 1:1 ratio. The mixture was filtered and concentrated in vacuo. The crude oil was then subjected to flash chromatography eluent: 1:1 hexane ethyl acetate, Rf=0.09. Single peak in LC-MS analysis, (1.3 g, 95% purity) and required no further purification; m/z (LC-MS, ESP), RT=3.66 mins (M+H) 481—compound cyclised on column

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902193B2
Source datasetuspto-grants-2011_03
ORD IDord-aad5ee53553d4a7fbbf55288cd14e8f9
Source noteuspto-grants-2011_03