Allylamine → HCID 20337907, compound
Reaction equation
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[CH:13][C:14]3[O:18][CH:17]([C:19](OCC)=[O:20])[CH2:16][C:15]=3[CH:24]=2)=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[CH2:25]([NH2:28])[CH:26]=[CH2:27]>C(O)C>[C:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:12]=[CH:13][C:14]3[O:18][CH:17]([C:19]([NH:28][CH2:25][CH:26]=[CH2:27])=[O:20])[CH2:16][C:15]=3[CH:24]=2)=[CH:9][CH:10]=1)(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
20 ml of ethanol was added to a mixture of 1.6 g of 7D and 20 ml of 2-propenylamine. The mixture was stirred for 3 hours at room temperature. The solid which formed was collected, washed with ethanol, then ether and dried under reduced pressure to give 7, mp: 244°-247° C.
Workup
- customThe solid which formed
- customwas collected
- washwashed with ethanol
- dry with materialether and dried under reduced pressure
- customto give 7, mp: 244°-247° C.
Sources & evidence
- ORD record
- ord-a8cfa7df2752454781c5cf66e655bb31
- Source dataset
- uspto-grants-1980_05
- Patent number
- US04205080
Reaction notes
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