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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272487Generated: October 26, 2026

Dopamine → 6-{[2-(3,4-Dihydroxy-phenyl)ethylamino]-methyl}-2,4-pteridinediamine

https://huagongshe.com/reaction/1272487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDopamineHCID 681—
ReactantBicarbonate IonHCID 769—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-(Bromomethyl)-2-imino-2,3-dihydropteridin-4-amine--hydrogen bromide (1/1)HCID 12503242—
SolventDimethylacetamideHCID 31374—
Product6-{[2-(3,4-Dihydroxy-phenyl)ethylamino]-methyl}-2,4-pteridinediamineHCID 1845572522.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-bromomethyl-2,4-pteridinediamine hydrobromide (67.3 mg, 0.2003 mmol) in anhydrous N,N dimethylacetamide was added 2-(3,4-dihydroxyphenyl) ethylamine (43.6 mg, 0.23 mmol). Under positive pressure of Argon, iPr2EtN (32.63 ul) was added. The reaction mixture was stirred at 50° C. for 4 hrs and then at Room temperature overnight. The crude product was poured into saturated bicarbonate solution. The resulted precipitate was collected and purified by preparative HPLC. 14.8 mg product was obtained. Yield: 22.6%; 1H NMR (500 MHz, DMSO-d6): δ 2.69242 (b, 4H), 4.03353 (s, 2H), 6.37542–6.39065 (d, J=7.615 Hz, 1H), 6.4851(s, 1H), 6.56632–6.58226 (d, J=7.97 Hz, 1H), 8.80972 (s, 1H); ESI-MS: m/z 328 (M++1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208493B2
Source datasetuspto-grants-2007_04
ORD IDord-09e79be0cd044caa97d569d8e6d6e144
Source noteuspto-grants-2007_04