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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388639Generated: October 30, 2026

DL-Tyrosine → HCID 21023684, compound

https://huagongshe.com/reaction/2388639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDL-TyrosineHCID 1153—
ReactantDiethylamineHCID 8021—
ReactantTetrahydrofuranHCID 8028—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
SolventDiethyl EtherHCID 3283—
ProductHCID 21023684HCID 2102368467%

Reaction Steps

To a solution of 2-amino-3-(4-hydroxyphenyl)propionic acid, (30.6 g, 0.129 mol) in THF (250 mL) at +10° C. was added 2,4-Dichloro-5-nitropyrimidine (25 g, 0.129 mol), keeping the temperature below 5° C. during the addition. Once the addition was complete, N,N-diisopropylethylamine (33.7 mL, 0.194 mol) was added dropwise. After stirring for 1 h at +10° C., diethylamine (66.73 mL, 0.645 mol) was added slowly, and then the reaction mixture was warmed to room temperature overnight. The reaction mixture was diluted with diethyl ether (500 mL), and the organic layer was washed with 0.2 N citric acid (3×150 mL), water (1×150 mL), and 10% K2CO3 (3×150 mL). The organic phase was dried (Na2SO4), filtered, and concentrated in vacuo to yield a yellow residue. The residue was purified by flash chromatography (20% EtOAc/hexanes on silica gel) to yield 37.39 g (67%) the title compound as a yellow foam. Rf=0.21 (25% EtOAc/hexanes on silica gel).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269009B2
Source datasetuspto-grants-2012_09
ORD IDord-01990aa5ffef4fa9ab425dd3f8714da6
Source noteuspto-grants-2012_09