4-(Chloromethyl)benzoyl chloride → HCID 22291056, compound

HRID 1369527Notes

Reaction equation

HRID 1369527 reaction equation
[Cl:1][CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.[NH2:12][C:13]1[CH:14]=[C:15]([NH:20][C:21](=[O:28])[C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:16]=[CH:17][C:18]=1[CH3:19]>>[C:21]([NH:20][C:15]1[CH:16]=[CH:17][C:18]([CH3:19])=[C:13]([NH:12][C:7](=[O:8])[C:6]2[CH:10]=[CH:11][C:3]([CH2:2][Cl:1])=[CH:4][CH:5]=2)[CH:14]=1)(=[O:28])[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

3

Reactant 2

HCID 701364-(Chloromethyl)benzoyl chlorideHCID 1120264N-(3-amino-4-methylphenyl)benzamide

Product 1

HCID 22291056HCID 22291056, compoundYield 99%

Procedure

Using an analogous procedure to that described in Example 37, 4-chloromethylbenzoyl chloride was reacted with N-(3-amino-4-methylphenyl)benzamide to give the title compound in 99% yield; NMR Spectrum: (DMSOd6) 2.19 (s, 3H), 4.84 (s, 2H), 7.22 (d, 1H), 7.54 (m, 6H), 7.84 (s, 1H), 7.96 (m, 4H), 9.92 (s, 1H), 10.22 (s, 1H); Mass Spectrum: M−H− 377.

Sources & evidence

ORD record
ord-ec23ecb770e14fa7bd36eefa0092bd22
Source dataset
uspto-grants-2003_06
Patent number
US06579872B1

Reaction notes

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