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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108276Generated: October 30, 2026

O-methyl-L-tyrosine N-Methylamide → 6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl ester

https://huagongshe.com/reaction/2108276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-methyl-L-tyrosine N-MethylamideHCID 14303038—
Reactant4-Methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acidHCID 53859812—
SolventDichloromethaneHCID 6344—
Product6-Methyl-4-[[[1-[(methylamino)carbonyl]-2-(4-methoxyphenyl)ethyl]amino]carbonyl]hept-3-enoic acid, methyl esterHCID 8511523453.3%

Reaction Steps

N,N-Dicyclohexylcarbodiimide (515 mg, 2.5 mmol) was added to an ice-cooled solution of 4-methoxycarbonyl-2-(2-methylpropyl)but-2-enoic acid (500 mg, 2.5 mmol) and O-methyl-L-tyrosine N-methylamide (520 mg, 2.5 mmol) in dry dichloromethane (30 ml), and the mixture was stirred at room temperature for 18 h. The precipitated solid was filtered off and washed with a little dichloromethane, then the organic solution was washed successively with 1N hydrochloric acid (20 ml), 1N sodium bicarbonate (20 ml), and water. The solution was dried (MgSO4) and evaporated in vacuo. Column chromatography (30 g silica) of the residual solid, eluting with 5% methanol/dichloromethane gave the title compound (520 mg, 53%), m.p. 142°-144° C. (dichloromethane/pentane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937243
Source datasetuspto-grants-1990_06
ORD IDord-5df8e4a4564241689f6433ba7df44eee
Source noteuspto-grants-1990_06