2,6-Dimethylbenzoyl chloride → HCID 19778032, compound

HRID 2082316Notes

Reaction equation

HRID 2082316 reaction equation
Cl.Cl.[N:3]1([C:8]2[CH:22]=[CH:21][C:11]([C:12]([N:14]3[CH2:19][CH2:18][CH:17]([NH2:20])[CH2:16][CH2:15]3)=[O:13])=[CH:10][CH:9]=2)[CH:7]=[CH:6][N:5]=[CH:4]1.[CH3:23][C:24]1[CH:32]=[CH:31][CH:30]=[C:29]([CH3:33])[C:25]=1[C:26](Cl)=[O:27]>>[N:3]1([C:8]2[CH:9]=[CH:10][C:11]([C:12]([N:14]3[CH2:19][CH2:18][CH:17]([NH:20][C:26](=[O:27])[C:25]4[C:29]([CH3:33])=[CH:30][CH:31]=[CH:32][C:24]=4[CH3:23])[CH2:16][CH2:15]3)=[O:13])=[CH:21][CH:22]=2)[CH:7]=[CH:6][N:5]=[CH:4]1

Participants

3

Reactant 2

HCID 890962,6-Dimethylbenzoyl chlorideHCID 19778043HCID 19778043, compound

Product 1

HCID 19778032HCID 19778032, compound

Procedure

In a manner similar to that described in Example 10, 1-[4-(1H-imidazol-1-yl)benzoyl]-4-piperidinamine dihydrochloride and 2,6-dimethylbenzoyl chloride are reacted to give the title compound.

Workup

  1. customare reacted

Sources & evidence

ORD record
ord-02d0939486514f3ea7a225edc70e274d
Source dataset
uspto-grants-1993_02
Patent number
US05189036

Reaction notes

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