2-Methoxyethylamine → HCID 86613128, compound
Reaction equation
[C:1](#[N:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:11][C:12]1[NH:16][N:15]=[C:14]([NH2:17])[CH:13]=1.[CH3:18][O:19][CH2:20][CH2:21][NH2:22]>>[CH3:18][O:19][CH2:20][CH2:21][NH:22][C:3]1[CH:2]=[C:1]([NH:17][C:14]2[CH:13]=[C:12]([CH3:11])[NH:16][N:15]=2)[N:10]=[C:1]([CH:2]=[CH:3][C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)[N:10]=1Participants
4
Procedure
Example 163 was synthesized via Scheme 6 according to the general scheme provided above with the appropriate starting materials cinnamonitrile, 5-methyl-1H-pyrazole-3-amine, and 2-methoxyethanamine. Structure of the target was confirmed by 1H-NMR. The 1H-NMR is attached.
Workup
- customExample 163 was synthesized via Scheme 6 according to the general scheme
- customprovided above with the
Sources & evidence
- ORD record
- ord-4c648f9e8a684f6a84a7fbbc5716a06b
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07563787B2
Reaction notes
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