Acetic Anhydride → HCID 11698006, compound

HRID 1178307Notes

Reaction equation

[OH:1][CH:2]1[C:19]([CH3:21])([CH3:20])[O:18][C:17]2[C:4](=[C:5]3[C:14](=[C:15]([O:22][CH3:23])[CH:16]=2)[C:13](=[O:24])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]4[CH:28]=[CH:27][CH:26]=[CH:25][C:11]4=2)[N:6]3[CH3:29])[C:3]1=[O:30].[C:31](OC(=O)C)(=[O:33])[CH3:32]>>[C:31]([O:1][CH:2]1[C:19]([CH3:20])([CH3:21])[O:18][C:17]2[C:4](=[C:5]3[C:14](=[C:15]([O:22][CH3:23])[CH:16]=2)[C:13](=[O:24])[C:12]2[C:7](=[CH:8][CH:9]=[C:10]4[CH:28]=[CH:27][CH:26]=[CH:25][C:11]4=2)[N:6]3[CH3:29])[C:3]1=[O:30])(=[O:33])[CH3:32]

Participants

Reactant 2

HCID 7918Acetic Anhydride

HCID 11516966HCID 11516966, compound

Product 1

HCID 11698006HCID 11698006, compound

Procedure

The compound is obtained according to the procedure of Example 14, starting from the compound of Example 16, using acetic anhydride instead of the butyryl chloride.

Workup

customThe compound is obtained

Sources & evidence

ORD record: ord-d33a2c52b53e4134afccc99f547a697a
Source dataset: uspto-grants-2007_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07276512B2

Reaction notes

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