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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852251Generated: October 26, 2026

Diisopropylethylamine → HCID 69376816, compound

https://huagongshe.com/reaction/852251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanine methyl esterHCID 11011855—
Reactant1-Chloro-2,6-naphthyridineHCID 12884774—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 69376816HCID 6937681647%

Reaction Steps

(S)-3-(4-Amino-phenyl)-2-tert-butoxycarbonylamino propionic acid methyl ester (574 mg, 1.95 mmol), 1-Chloro-2,6-naphthyridine (350 mg, 2.13 mmol) (prepared according to the method of Van der Plas, H. C. et al J. Heterocyclic Chem. 1981, 18, 1349) and DIPEA (372 μl, 2.13 mmol) in 2-ethoxyethanol (0.5 ml) were stirred at 130° C. under N2 overnight. The reaction mixture was partitioned between EtOAc (70 ml) and saturated aqueous NaHCO3 (30 ml). The phases were separated and the aqueous layer re-extracted with EtOAc (3×30 ml). The combined organic extracts were dried (MgSO4) and the solvents eliminated in vacuo. The residue was purified by flash chromatography (5:1 to 1:1 hexanes/EtOAc) to give (S)-2-tert-butoxycarbonylamino-3-[4-([2,6]naphthyridin-1-ylamino)phenyl] propionic acid methyl ester (385 mg, 47%) as an orange foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253171B2
Source datasetuspto-grants-2007_08
ORD IDord-7970129eae984432b7ee9dc187f7233c
Source noteuspto-grants-2007_08