Guanosine → HCID 136341907, compound

HRID 969771Notes

Reaction equation

HRID 969771 reaction equation
[C:1]([C@@:18]1([N:26]2[C:36]3[N:35]=[C:33]([NH2:34])[NH:32][C:30](=[O:31])[C:29]=3[N:28]=[CH:27]2)[O:25][C@H:22]([CH2:23][OH:24])[C@@H:20]([OH:21])[CH2:19]1)(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[C@@H]1(N2C3N=C(N)NC(=O)C=3N=C2)O[C@H](CO)[C@@H](O)[C@H]1[OH:39].O.[C@@H]1(N2C3N=C(N)NC(=O)C=3N=C2)O[C@H](CO)[C@@H](O)C1>>[C:1]([C@@:18]1([N:26]2[C:36]3[N:35]=[C:33]([NH2:34])[NH:32][C:30](=[O:31])[C:29]=3[N:28]=[CH:27]2)[O:25][C@H:22]([CH2:23][OH:24])[C@@H:20]([OH:21])[C@H:19]1[OH:39])(=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]

Participants

4

Reactant 3

HCID 135398635GuanosineHCID 1354457052'-Deoxyguanosine monohydrateHCID 136333583HCID 136333583, compound

Product 1

HCID 136341907HCID 136341907, compound

Procedure

This compound was prepared using the procedure for palmitoyl-2′-deoxyguanosine, substituting the appropriate amount of guanosine 2′,3′-acylic dialcohol for 2′-deoxyguanosine monohydrate.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-12f1c06126ad409c974dee4aa2a32b68
Source dataset
uspto-grants-2007_12
Patent number
US07307166B1

Reaction notes

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