HCID 18357678, compound → HCID 9859697, compound
Reaction equation
[C:1](O)(=O)/C=C\C(O)=O.O1C2=N[CH:15]=[CH:16][CH:17]=[C:12]2[C:11]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[CH:24]([CH2:26][C:27]#[CH:28])[NH2:25])=N1.O1C2=NC=CC=C2[C:31](C2C=CC=CC=2C=O)=[N:30]1>>[C:31]([C:15]1[CH:1]=[C:11]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[CH:24]([CH2:26][C:27]#[CH:28])[NH2:25])[CH:12]=[CH:17][CH:16]=1)#[N:30]Participants
3
Procedure
2-(isoxazolo[5,4-b]pyridin-3-yl)-a-2-propynyl-benzenemethanamine (Z)-butenedioate starting from 2-(isoxazolo[5,4-b]pyridin-3-yl)-benzaldehyde, melting at 180-185° C. (dec).
Sources & evidence
- ORD record
- ord-297b26aa87f341ddae43b216524e5e7d
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06080773
Reaction notes
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