3-Bromopentane → HCID 68984566, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([C:10]2[O:11][CH:12]=[C:13]([CH2:15][NH:16][C:17](=[O:27])[C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[O:24][CH2:25][CH3:26])[N:14]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].Br[CH:29]([CH2:32][CH3:33])[CH2:30][CH3:31]>>[CH2:25]([O:24][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=1[C:17]([NH:16][CH2:15][C:13]1[N:14]=[C:10]([C:4]2[CH:5]=[CH:6][C:7]([O:8][CH3:9])=[C:2]([O:1][CH:29]([CH2:32][CH3:33])[CH2:30][CH3:31])[CH:3]=2)[O:11][CH:12]=1)=[O:27])[CH3:26]Participants
3
Procedure
Using the compound obtained in Example 2 and 3-bromopentane, white powdery 2-ethoxy-N-{2-[3-(1-ethylpropoxy)-4-methoxyphenyl]oxazol-4-ylmethyl}benzamide was obtained following the procedure of Example 3.
Sources & evidence
- ORD record
- ord-452a4b6afbb84a9c85703060e06e02f8
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08637559B2
Reaction notes
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