Acetic Anhydride → HCID 178476360, compound

HRID 1578356Notes

Reaction equation

[CH:1]1([NH:7][C:8]2[N:9]=[C:10]([OH:26])[C:11]3[N:12]=[CH:13][N:14]([C:24]=3[N:25]=2)[C@@H:15]2[O:23][C@H:20]([CH2:21][OH:22])[C@@H:18]([OH:19])[C@H:16]2[OH:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(O[C:31](=[O:33])[CH3:32])(=O)C>>[CH:1]1([NH:7][C:8]2[N:9]=[C:10]([OH:26])[C:11]3[N:12]=[CH:13][N:14]([C:24]=3[N:25]=2)[C@@H:15]2[O:23][C@H:20]([CH2:21][O:22][C:31](=[O:33])[CH3:32])[C@@H:18]([O:19][C:18](=[O:19])[CH3:20])[C@H:16]2[O:17][C:16](=[O:17])[CH3:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Participants

Reactant 2

HCID 7918Acetic Anhydride

HCID 178521068HCID 178521068, compound

Product 1

HCID 178476360HCID 178476360, compound

Procedure

By a procedure similar to that of Example 4(a), 1 part by weight of 2-cyclohexylaminoinosine is reacted with 5 parts by volume of acetic anhydride to obtain 1.1 parts by weight of 2-cyclohexylamino-2',3',5'-tri-O-acetylinosine as a colorless resinous product.

Sources & evidence

ORD record: ord-b15b619f215f41e886cf7f40fdf2b50f
Source dataset: uspto-grants-1976_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US03936439

Reaction notes

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