Allylamine → HCID 20383071, compound
Reaction equation
[CH: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)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:20]([NH2:23])[CH:21]=[CH2:22]>>[CH: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)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
3
Procedure
5 Also was prepared, as white crystals, mp: 93°-94° C., by the procedure described in the last paragraph of Example 2, from the ethyl ester of 6-cyclohexyl-3,4-dihydro-2H-1-benzopyran-2-carboxylic acid (Witiak et al. (1975)) and 2-propenamine.
Workup
- custom5 Also was prepared, as white crystals, mp: 93°-94° C., by the procedure
Sources & evidence
- ORD record
- ord-37eb3bac8b1e4a5fb5e1003541a75e6b
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04178380
Reaction notes
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