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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012956Generated: October 30, 2026

Triethylamine → 2-{3-[2-Fluoro-5-(4-oxo-3,4,5,6,7,8-hexahydro-phthalazin-1-ylmethyl)-phenyl]-ureido}-propionic Acid Methyl Ester

https://huagongshe.com/reaction/1012956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
Reactant2-Fluoro-5-(4-oxo-3,4,5,6,7,8-hexahydro-phthalazin-1-ylmethyl)-benzoic acidHCID 25005019—
SolventAcetonitrileHCID 6342—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-{3-[2-Fluoro-5-(4-oxo-3,4,5,6,7,8-hexahydro-phthalazin-1-ylmethyl)-phenyl]-ureido}-propionic Acid Methyl EsterHCID 57786640—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 2-fluoro-5-(4-oxo-3,4,5,6,7,8-hexahydro-phthalazin-1-ylmethyl)benzoic acid (11) (0.50 g, 1.650 mmol), in acetonitrile (2.5 ml) was added triethylamine (0.46 ml, 3.31 mmol) the suspension dissolved to afford a brown solution which was subsequently heated to 85° C. D/L alanine methyl ester hydrochloride (2.30 g, 1.650 mmol) dissolved in acetonitrile (5 ml) and N-methylpyrrolidinone (0.5 ml) was added simultaneously to the reaction mixture with diphenylphosphinic azide (0.357 ml, 1.650 mmol). After 40 minutes of heating the reaction mixture was cooled to ambient temperature and concentrated to vacuo. The crude oil was then subjected to flash chromatography, eluent hexane/ethyl acetate, 7:13 (Rf=0.14). Single peak in LC-MS, (0.67 g, 98% purity); m/z (LC-MS, ESP), RT=3.37 mins (M+H 403.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981890B2
Source datasetuspto-grants-2011_07
ORD IDord-f745de5a42854b289975365c67a7309a
Source noteuspto-grants-2011_07