1-(3-Methyl-1,2,4-thiadiazol-5-yl)piperidin-4-one → HCID 53353238, compound

HRID 451393Notes

Reaction equation

HRID 451393 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.[F:14][C:15]1[CH:16]=[C:17]([CH:25]=[C:26]([F:29])[C:27]=1[F:28])[CH2:18][N:19]1[CH:23]=[CH:22][C:21]([NH2:24])=[N:20]1>>[F:29][C:26]1[CH:25]=[C:17]([CH:16]=[C:15]([F:14])[C:27]=1[F:28])[CH2:18][N:19]1[CH:23]=[CH: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 673429711-(3,4,5-Trifluoro-benzyl)-1H-pyrazol-3-ylamine

Product 1

HCID 53353238HCID 53353238, 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-(3,4,5-trifluoro-benzyl)-1H-pyrazol-3-ylamine. The title compound was obtained as a colorless oil (yield=42%).

Workup

  1. customPrepared in analogy to example 1 step h)

Sources & evidence

ORD record
ord-1a7bebf70bbc49e49ac9ca051aadfec9
Source dataset
uspto-grants-2013_07
Patent number
US08486967B2

Reaction notes

Loading…