1-(3-Methyl-1,2,4-thiadiazol-5-yl)piperidin-4-one → HCID 53354636, compound

HRID 451381Notes

Reaction equation

HRID 451381 reaction equation
[CH3:1][C:2]1[N:6]=[C:5]([N:7]2[CH2:12][CH2:11][C:10](=O)[CH2:9][CH2:8]2)[S:4][N:3]=1.[Cl:14][C:15]1[CH:16]=[C:17]([CH:25]=[C:26]([Cl:28])[CH:27]=1)[CH2:18][N:19]1[CH:23]=[N:22][C:21]([NH2:24])=[N:20]1>>[Cl:28][C:26]1[CH:25]=[C:17]([CH:16]=[C:15]([Cl:14])[CH:27]=1)[CH2:18][N:19]1[CH:23]=[N:22][C:21]([NH:24][CH:10]2[CH2:11][CH2:12][N:7]([C:5]3[S:4][N:3]=[C:2]([CH3:1])[N:6]=3)[CH2:8][CH2:9]2)=[N:20]1

Participants

3

Reactant 2

HCID 592585101-(3-Methyl-1,2,4-thiadiazol-5-yl)piperidin-4-oneHCID 67345090HCID 67345090, compound

Product 1

HCID 53354636HCID 53354636, compound

Procedure

Prepared in analogy to example 1 step h) starting from 1-(3-methyl-[1,2,4]thiadiazol-5-yl)-piperidin-4-one (example 1c) and 1-(3,5-dichloro-benzyl)-1H-[1,2,4]triazol-3-ylamine. The title compound was obtained as a white solid (yield=27%).

Workup

  1. customPrepared in analogy to example 1 step h)

Sources & evidence

ORD record
ord-9cb0e1a042144d3c9a9d9cc80fbc6449
Source dataset
uspto-grants-2013_07
Patent number
US08486967B2

Reaction notes

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