4-Chlorobutyryl chloride → 2-Benzyl-1-(4-chlorobutyrylamino)-6-methylbenzene
Reaction equation
[CH2:1]([C:8]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:9]=1[NH2:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:16][CH2:17][CH2:18][CH2:19][C:20](Cl)=[O:21]>>[CH2:1]([C:8]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:9]=1[NH:10][C:20](=[O:21])[CH2:19][CH2:18][CH2:17][Cl:16])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
2-benzyl-6-methylaniline and 4-chlorobutyryl choride were used to produce the above compound in the same way as Reference Example 8.
Workup
- customto produce the above compound in the same way as Reference Example 8
Sources & evidence
- ORD record
- ord-52a0973dcc1647d6b5bf02c79809d649
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05723475
Reaction notes
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