HCID 20516151, compound → HCID 20516037, compound

HRID 1902343Notes

Reaction equation

HRID 1902343 reaction equation
[NH2:1][C:2]1[C:15]([CH2:16][N:17]([CH2:20][CH3:21])[CH2:18][CH3:19])=[CH:14][C:5]([C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12]Cl)=[O:7])=[CH:4][C:3]=1[Br:22].[C:23]([C:31]1[CH:32]=[C:33]([CH:37]([CH3:41])[C:38]([O-:40])=[O:39])[CH:34]=[CH:35][CH:36]=1)(=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[Na+]>>[NH2:1][C:2]1[C:15]([CH2:16][N:17]([CH2:20][CH3:21])[CH2:18][CH3:19])=[CH:14][C:5]([C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][O:40][C:38](=[O:39])[CH:37]([C:33]2[CH:34]=[CH:35][CH:36]=[C:31]([C:23](=[O:30])[C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH:32]=2)[CH3:41])=[O:7])=[CH:4][C:3]=1[Br:22]

Participants

3

Reactant 2

HCID 20516151HCID 20516151, compoundHCID 23684815Sodium 2-(3-benzoylphenyl)propanoate

Product 1

HCID 20516037HCID 20516037, compound

Procedure

This compound was prepared from 4-(4-amino-3-bromo-5-diethylaminomethyl-benzoyloxy)-n-butyl chloride and sodium 3-benzoyl-α-methyl-phenylacetate analogous to Example 8.

Sources & evidence

ORD record
ord-97e01c35aaed44b0a71ce2668bb7632f
Source dataset
uspto-grants-1982_12
Patent number
US04362738

Reaction notes

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