2-Methylindolizine → HCID 68848554, compound

HRID 1987841Notes

Reaction equation

HRID 1987841 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[N:9]([CH:10]=1)[CH:8]=[CH:7][CH:6]=[CH:5]2.[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[N+:22]([O-:24])=[O:23])[C:16](Cl)=[O:17]>>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([C:16]([C:10]2[N:9]3[C:4]([CH:5]=[CH:6][CH:7]=[CH:8]3)=[CH:3][C:2]=2[CH3:1])=[O:17])[CH:19]=[CH:20][C:21]=1[N+:22]([O-:24])=[O:23]

Participants

3

Reactant 2

HCID 5826302-MethylindolizineHCID 111276553-methoxy-4-nitro-benzoyl Chloride

Product 1

HCID 68848554HCID 68848554, compound

Procedure

This compound is obtained by carrying out the procedure according to the preparation described in Example 1, by benzoylation of 2-methylindolizine, described in Pharmazie; (1980), vol 35(4), pp 203-204, with 3-methoxy-4-nitrobenzoyl chloride.

Workup

  1. customThis compound is obtained

Sources & evidence

ORD record
ord-fd054c86e62c4f6ba553cf1c21f7766b
Source dataset
uspto-grants-2009_06
Patent number
US07553845B2

Reaction notes

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