But-2-yn-1-amine hydrochloride → HCID 22597423, compound
Reaction equation
[ClH:1].[NH2:2][C:3]1[N:11]=[C:10](C#CC(O)(C)C)[N:9]=[C:8]2[C:4]=1[N:5]=[C:6]([C:25]1[CH:30]=[CH:29][CH:28]=[C:27](F)[CH:26]=1)[N:7]2[C:18]1[CH:19]=[CH:20][C:21](=[O:24])[NH:22][CH:23]=1.Cl.[CH2:33](N)C#CC>>[ClH:1].[NH2:2][C:3]1[N:11]=[CH:10][N:9]=[C:8]2[C:4]=1[N:5]=[C:6]([C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([Cl:1])[CH:26]=1)[N:7]2[C:18]1[CH:19]=[CH:20][C:21](=[O:24])[N:22]([CH3:33])[CH:23]=1Participants
3
Procedure
The title compound was synthesized in the same manner as in Example 1 (2), (3) and (4), and Examples 2 and 5.
Sources & evidence
- ORD record
- ord-24e73c13a0384248b5ab31ad437fd8c4
- Source dataset
- uspto-grants-2005_01
- Patent number
- US06841549B1
Reaction notes
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