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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469874Generated: October 29, 2026

Acetonitrile → (S)-2-amino-3-(4-(5-(naphthalen-2-ylmethylamino)pyrazin-2-yl)phenyl)propanoic acid

https://huagongshe.com/reaction/469874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
Reactant5-bromo-N-(naphthalen-2-ylmethyl)pyrazin-2-amineHCID 86614307—
CatalystPalladium(2+);triphenylphosphane;dichlorideHCID 22065850—
SolventWaterHCID 962—
Product(S)-2-amino-3-(4-(5-(naphthalen-2-ylmethylamino)pyrazin-2-yl)phenyl)propanoic acidHCID 24894502—

Reaction Steps

5-Bromo-N-(naphthalen-2-ylmethyl)pyrazin-2-amine (0.2 g, 0.637 mmol), L-p-boronophenylalanine (0.13 g, 0.637 mmol), palladiumtriphenylphosphine dichloride (13 mg, 0.019 mmol), Na2CO3 (0.13 g, 1.27 mmol), acetonitrile (5 mls) and water (5 mls) were heated in a microwave reactor at 150° C. for 5 minutes. The mixture was concentrated, dissolved in 1.0 N HCl, washed twice with ether, concentrated, dissolved in methanol, filtered and concentrated to yield 0.12 g of the captioned compound. M+1=399; 1H NMR (CD3OD) δ 8.51 (s, 1H), 8.37 (s, 1H), 7.90 (m, 6H), 7.50 (m, 5H), 4.85 (s, 2H), 4.30 (t, 1H), 3.38 (m, 1H), 3.22 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629156B2
Source datasetuspto-grants-2014_01
ORD IDord-584bab270fe34a04bc04bf797b41e6a8
Source noteuspto-grants-2014_01