Dimethylformamide → Methyl 4-{6-amino-8-(3-fluorophenyl)-2-[2-(1-hydroxycyclohexyl)-1-ethynyl]-9H-9-purinyl}butanoate

HRID 1826540

Reaktionsgleichung

[NH2:1][C:2]1[N:10]=[C:9](I)[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=1)[N:6]2[CH2:12][CH2:13][CH2:14][C:15]([O:17][CH3:18])=[O:16].CN(C)C=O.[CH2:31]([C:33]1([OH:39])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1)[CH3:32]>[Cu]I.C(N(CC)CC)C>[NH2:1][C:2]1[N:10]=[C:9]([C:32]#[C:31][C:33]2([OH:39])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]2)[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=1)[N:6]2[CH2:12][CH2:13][CH2:14][C:15]([O:17][CH3:18])=[O:16]

Komponenten

Reaktionsbedingungen

Temperatur: 70 °C

Versuchsvorschrift

To 162 mg of methyl 4-[6-amino-8-(3-fluorophenyl)-2-iodo-9H-9-purinyl]butanoate were added 8 ml of N,N-dimethylformamide, 30 mg of copper(I) iodide, 30 mg of dichlorobis(triphenylphosphine)palladium(II)l, 80 mg of 1-ethylcyclohexanol and 74 μl of triethylamine and the mixutre was stirred in a nitrogen stream at 70° C. for 2.5 hours. After it was allowed to cool, the solvent was evaporated and the resulting reside was subjected to a silica gel column chromatography (25 g of silica gel; chloroform-methanol (100:0-100:1-50:1) to give 144 mg of the title compound. The yield was 90%.

Aufarbeitung

temperatureto cool
customthe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag: ord-b78d0325173645d69b871303a936fe98
Quelldatensatz: uspto-grants-2006_05
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: USRE039112E1

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