STK173631 → HCID 19423560, compound

HRID 743071Notes

Reaction equation

HRID 743071 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([NH:16][C:17](=[O:22])C(Cl)(Cl)Cl)=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=O.[NH2:23][CH:24]1[CH2:29][CH2:28][N:27]([CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[CH2:26][CH2:25]1>>[CH2:30]([N:27]1[CH2:28][CH2:29][CH:24]([N:23]2[CH:7]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:6]3[C:5](=[CH:4][CH:3]=[C:2]([Cl:1])[CH:15]=3)[NH:16][C:17]2=[O:22])[CH2:25][CH2:26]1)[C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1

Participants

3

Reactant 2

HCID 306974STK173631HCID 4158521-Benzyl-4-piperidylamine

Product 1

HCID 19423560HCID 19423560, compound

Procedure

In similar way as in Preparation Example 24, the title compound was synthesized from 5-chloro-2-trichloroacetylaminobenzophenone and 4-amino-1-benzylpiperidine.

Workup

  1. customIn similar way as in Preparation Example 24

Sources & evidence

ORD record
ord-c7cdc72bee664ee1a51ba13af457d137
Source dataset
uspto-grants-1996_09
Patent number
US05556860

Reaction notes

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