Chloroacetyl chloride → 2-[(2-Methyl-4-(chloroacetamido)phenyl)amino]-1-pyrroline, hydrochloride
Reaction equation
[Cl:1][CH2:2][C:3](Cl)=[O:4].Cl.Cl.[CH3:8][C:9]1[CH:14]=[C:13]([NH2:15])[CH:12]=[CH:11][C:10]=1[NH:16][C:17]1[CH2:21][CH2:20][CH2:19][N:18]=1>>[ClH:1].[CH3:8][C:9]1[CH:14]=[C:13]([NH:15][C:3](=[O:4])[CH2:2][Cl:1])[CH:12]=[CH:11][C:10]=1[NH:16][C:17]1[CH2:21][CH2:20][CH2:19][N:18]=1Participants
3
Procedure
The title compound was prepared by the method of Example 16 using 30.5 mmole of chloroacetyl chloride and 1.0 g (3.8 mmole) of the product compound of Example 9. Structure assignment was supported by the nmr spectrum and by elemental analysis.
Sources & evidence
- ORD record
- ord-d2aabcae855f4582951746657ba9d6af
- Source dataset
- uspto-grants-1985_08
- Patent number
- US04533739
Reaction notes
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