Hexanoyl chloride → HCID 11660406, compound
Reaction equation
[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[S:11][C:10]([NH2:12])=[N:9][C:8]=2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:4][N:3]=1.[C:19](Cl)(=[O:25])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]>>[CH3:1][C:2]1[N:6]=[C:5]([C:7]2[S:11][C:10]([NH:12][C:19](=[O:25])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[N:9][C:8]=2[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[O:4][N:3]=1Participants
3
Procedure
Prepared from 5-(3-methyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-ylamine and hexanoyl chloride.
Sources & evidence
- ORD record
- ord-c133364fc50747bf96e75ba3338d9ffa
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910613B2
Reaction notes
Loading…