Acetic Anhydride → 10-Acetoxy-5,5-dimethyl-8-iso-propyl-5H-[1]benzopyrano[3,4-d]pyridine
Reaction equation
[CH3:1][C:2]1([CH3:20])[C:15]2=[CH:16][CH:17]=[N:18][CH:19]=[C:14]2[C:5]2[C:6]([OH:13])=[CH:7][C:8]([CH:10]([CH3:12])[CH3:11])=[CH:9][C:4]=2[O:3]1.[C:21](OC(=O)C)(=[O:23])[CH3:22]>N1C=CC=CC=1>[C:21]([O:13][C:6]1[C:5]2[C:14]3[C:15]([C:2]([CH3:1])([CH3:20])[O:3][C:4]=2[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[CH:7]=1)=[CH:16][CH:17]=[N:18][CH:19]=3)(=[O:23])[CH3:22]Participants
4
Procedure
10-Acetoxy-5,5-dimethyl-8-iso-propyl-5H-[1]benzopyrano[3,4-d]pyridine is prepared by reacting 5,5-dimethyl-10-hydroxy-8-iso-propyl-5H-[1]benzopyrano[3,4-d]pyridine and acetic anhydride in the presence of pyridine according to the method of Example 12.
Sources & evidence
- ORD record
- ord-b9f2c7db3e934c41a6f6c761e0b7bfc5
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04254116
Reaction notes
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