Piperonylamine → HCID 20484283, compound
Reaction equation
Cl.[NH:2]([C:4]1[CH:5]=[CH:6][C:7]2[S:11][CH:10]=[C:9]([CH3:12])[C:8]=2[CH:13]=1)N.O.Cl.[NH:16]1[CH2:21][CH2:20][C:19](=O)[CH2:18][CH2:17]1>>[CH3:12][C:9]1[C:8]2=[C:13]3[C:4](=[CH:5][CH:6]=[C:7]2[S:11][CH:10]=1)[NH:2][C:19]1[CH2:20][CH2:21][NH:16][CH2:17][C:18]3=1Participants
3
Procedure
The compound is formed analogously to that described in Example 2, from 5 g of 5-hydrazino-3-methylbenzothiophene hydrochloride and 5 g of 4-piperidone hydrochloride monohydrate. Melting point: 234° C.
Workup
- customThe compound is formed analogously to that
Sources & evidence
- ORD record
- ord-316dbbec612c40eb8700834914f82bf4
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04410536
Reaction notes
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