HCID 54073826, compound → HCID 20223684, compound

HRID 1249628Notes

Reaction equation

HRID 1249628 reaction equation
[CH2:1]([O:8][C:9]1[C:10]([CH3:30])=[N+:11]([O-])[C:12]([CH:15]([O:25][C:26](=[O:28])[CH3:27])[CH2:16][N:17]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:18](=[O:20])[CH3:19])=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(OC(=O)C)(=O)C>[C:26]([O:28][CH2:30][C:10]1[C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:14][CH:13]=[C:12]([CH:15]([O:25][C:26](=[O:28])[CH3:27])[CH2:16][N:17]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:18](=[O:20])[CH3:19])[N:11]=1)(=[O:25])[CH3:27]

Participants

3

Reactant 1

HCID 54073826HCID 54073826, compound

Product 1

HCID 20223684HCID 20223684, compound

Reagents, catalysts & solvents 1

HCID 7918Acetic AnhydrideSolvent

Procedure

3-Benzyloxy-2-methyl-6-[1-acetoxy-2-(N-tert-butylacetamido)ethyl]pyridine N-oxide is heated in acetic anhydride according to the method of Example 21 to produce 2-acetoxymethyl-3-benzyloxy-6-[1-acetoxy-2-(N-tert-butylacetamido)ethyl]pyridine.

Sources & evidence

ORD record
ord-06c0fd2f7f0f4d73ae0382adc985fec5
Source dataset
uspto-grants-1986_12
Patent number
US04632992

Reaction notes

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