trans-3-(3-Pyridyl)acrylic acid → HCID 20613739, compound
Reaction equation
Cl.Cl.[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH2:11])[CH2:4]2.[N:12]1[CH:17]=[CH:16][CH:15]=[C:14](/[CH:18]=[CH:19]/[C:20](O)=[O:21])[CH:13]=1>>[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH:11][C:20](=[O:21])/[CH:19]=[CH:18]/[C:14]1[CH:13]=[N:12][CH:17]=[CH:16][CH:15]=1)[CH2:4]2Participants
3
Procedure
Prepared as a free base by a method analogous to that described in Example 1 from (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride and E-3-(3-pyridyl)propenoic acid; the compound was purified by chromatography on silica gel using ammoniated methanol/chloroform mixtures as the eluent; MS (ES+) 258 (MH+).
Workup
- customPrepared as a free base by a method analogous to
- customthe compound was purified by chromatography on silica gel using ammoniated methanol/chloroform mixtures as the eluent
Sources & evidence
- ORD record
- ord-31d10ca859454701ad4f228a5bfa9eeb
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683090B1
Reaction notes
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