2-Amino-1-butanol, (-)- → 3-{4-[6-(1-Hydroxymethyl-propylamino)-2-oxo-3-propyl-3,7-dihydro2H-purin-8-yl]-bicyclo[2.2.2]oct-1-yl]-propionic acid methyl ester

HRID 1793821Notes

Reaction equation

[CH3:1][O:2][C:3](=[O:29])[CH2:4][CH2:5][C:6]12[CH2:13][CH2:12][C:9]([C:14]3[NH:22][C:21]4[C:20](SC)=[N:19][C:18](=[O:25])[N:17]([CH2:26][CH2:27][CH3:28])[C:16]=4[N:15]=3)([CH2:10][CH2:11]1)[CH2:8][CH2:7]2.[NH2:30][C@H:31]([CH2:34][CH3:35])[CH2:32][OH:33]>CS(C)=O>[CH3:1][O:2][C:3](=[O:29])[CH2:4][CH2:5][C:6]12[CH2:13][CH2:12][C:9]([C:14]3[NH:22][C:21]4[C:20]([NH:30][CH:31]([CH2:32][OH:33])[CH2:34][CH3:35])=[N:19][C:18](=[O:25])[N:17]([CH2:26][CH2:27][CH3:28])[C:16]=4[N:15]=3)([CH2:10][CH2:11]1)[CH2:8][CH2:7]2

Participants

Conditions

Temperature: 150 °C

Procedure

3-[4-(6-Methylsulfanyl-2-oxo-3-propyl-3,7-dihydro-2H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-propionic acid methyl ester (105 mg) was dissolved in 2 mL of DMSO along with an appropriate amino alcohol (e.g., 160 uL of (R)-2-amino-1-butanol for compound 3). The reaction mixture was stirred at 150° C. for 3 h. It was then cooled to rt and purified by preparative HPLC to afford 50 mg of the titled compound.

Workup

temperatureIt was then cooled to rt
custompurified by preparative HPLC

Sources & evidence

ORD record: ord-1e7398f86ebd47c2b797ef9a88162610
Source dataset: uspto-grants-2006_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07022686B2

Reaction notes

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