Sulfanilamide → N,N-Bis(2-methylpropyl)prop-1-en-1-amine
Reaction equation
ClC1C=CC(C(=O)[CH2:7][CH:8]([CH3:11])[CH:9]=O)=CC=1.S(C1[CH:25]=[CH:24][C:22]([NH2:23])=CC=1)(=O)(=O)N>>[CH2:7]([N:23]([CH:22]=[CH:24][CH3:25])[CH2:9][CH:8]([CH3:7])[CH3:11])[CH:8]([CH3:11])[CH3:9]Participants
3
Procedure
Following a procedure similar to that described in Example 64(iii), but using 2-(4-chlorophenacyl) propionaldehyde [prepared as described in step (ii) above] and 4-sulfamoylaniline as starting materials, the title compound was obtained as a pale brown powder (yield 35%), melting at 196-198° C.
Sources & evidence
- ORD record
- ord-fa19c9d871d2448f997d265c8f3c0644
- Source dataset
- uspto-grants-2006_12
- Patent number
- USRE039420E1
Reaction notes
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