Acetic Anhydride → HCID 69274266, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5](/[CH:8]=[C:9](/[C:12]2[CH:17]=[C:16]([O:18][CH3:19])[C:15]([O:20][CH3:21])=[C:14]([O:22][CH3:23])[CH:13]=2)\[C:10]#[N:11])=[CH:4][CH:3]=1.[C:24](OC(=O)C)(=[O:26])[CH3:25]>N1C=CC=CC=1>[C:24]([O:1][C:2]1[CH:7]=[CH:6][C:5](/[CH:8]=[C:9](\[C:10]#[N:11])/[C:12]2[CH:13]=[C:14]([O:22][CH3:23])[C:15]([O:20][CH3:21])=[C:16]([O:18][CH3:19])[CH:17]=2)=[CH:4][CH:3]=1)(=[O:26])[CH3:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 15 (1.20 g) was acetylated with acetic anhydride and pyridine in accordance with a customary method, to thereby produce the target product (1.27 g, yield: 93%).
Sources & evidence
- ORD record
- ord-14babc7669b54d06903cd35f0676de21
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371773B2
Reaction notes
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