Allylamine → HCID 20383067, compound
Reaction equation
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:15][CH:14]([C:16]([OH:18])=O)[CH2:13][CH2:12][C:11]=3[CH:19]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20]([NH2:23])[CH:21]=[CH2:22]>>[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:15][CH:14]([C:16]([NH:23][CH2:20][CH:21]=[CH2:22])=[O:18])[CH2:13][CH2:12][C:11]=3[CH:19]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
4 Was prepared as a white solid, mp: 123°-124° C. from the ethyl ester of 3,4-dihydro-6-phenyl-2H-1-benzopyran-2-carboxylic acid (Witiak et al. (1975)) and 2-propenamine by the procedure described in the last paragraph of Example 2.
Sources & evidence
- ORD record
- ord-0ed1e2e8174647b784e3b2dcca841204
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04178380
Reaction notes
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