Butyl bromide → Diethyl [5-(7-butyl-3-methylxanthin-1-yl)pentyl]phosphonate

HRID 2038

Reaction equation

HRID 2038 reaction equation
[CH3:1][N:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[C:5](=[O:11])[N:4]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][P:17](=[O:24])([O:21][CH2:22][CH3:23])[O:18][CH2:19][CH3:20])[C:3]1=[O:25].Br[CH2:27][CH2:28][CH2:29][CH3:30]>>[CH2:27]([N:7]1[C:6]2[C:5](=[O:11])[N:4]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][P:17](=[O:24])([O:21][CH2:22][CH3:23])[O:18][CH2:19][CH3:20])[C:3](=[O:25])[N:2]([CH3:1])[C:10]=2[N:9]=[CH:8]1)[CH2:28][CH2:29][CH3:30]

Participants

3

Procedure

The title substance was prepared from 0.008 mol of diethyl [5-(3-methyl-xanthin-1-yl)pentyl]phosphonate and 0.01 mol of 1-bromobutane analogously to Example 46.

Sources & evidence

ORD record
ord-e9220e2450c24e59bc6ac895e81aca07
Source dataset
uspto-grants-1998_03
Patent number
US05728686

Linked notes

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