3-Butyn-1-OL → HCID 86690328, compound
Reaction equation
[NH2:1][C:2]1[C:3](C#CCCCCC(O)=O)=[N:4][C:5]([C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[N:7]=1.[CH2:31]([OH:35])[CH2:32][C:33]#[CH:34]>>[NH2:1][C:2]1[C:3]([C:34]#[C:33][CH2:32][CH2:31][OH:35])=[N:4][C:5]([C:15]2[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=2)=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[N:7]=1Participants
3
Procedure
The title compound was prepared analogously to 7-(3-amino-5,6-di-p-tolylpyrazin-2-yl)hept-6-ynoic acid (Ex 7 step 1) by replacing hept-6-ynoic acid with but-3-yn-1-ol;
Sources & evidence
- ORD record
- ord-0ec872c8421a4a2ca5340961801a7ce9
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937069B2
Reaction notes
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