4-Amino-1-methylpiperidine → HCID 86695320, compound

HRID 572823Notes

Reaction equation

HRID 572823 reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH2:19][CH2:20][CH3:21])[CH:13]=1)=O.[NH2:22][CH:23]1[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]1>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10](=[N:22][CH:23]1[CH2:28][CH2:27][N:26]([CH3:29])[CH2:25][CH2:24]1)[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH2:19][CH2:20][CH3:21])[CH:13]=1

Participants

3

Procedure

Condensation of benzothiazol-2-yl(3-propoxyphenyl)methanone with 4-amino-1-methylpiperidine as described in example 37B gives [benzothiazol-2-yl(3-propoxyphenyl)methylene](1-methylpiperidin-4-yl)amine.

Sources & evidence

ORD record
ord-9f4a2c8eebc0470c9527bf39387e8e06
Source dataset
uspto-grants-2015_05
Patent number
US09029357B2

Reaction notes

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