N-Ethylpyridine-2-ethylamine → HCID 59577914, compound
Reaction equation
[O:1]=[C:2]1[C:6]2([CH2:11][CH2:10][N:9]([S:12](Cl)(=[O:14])=[O:13])[CH2:8][CH2:7]2)[CH2:5][CH2:4][N:3]1[C:16]1[CH:21]=[CH:20][C:19]([O:22][C:23]([F:26])([F:25])[F:24])=[CH:18][CH:17]=1.C(N[CH2:30][CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=1)C>>[CH2:34]([NH:33][S:12]([N:9]1[CH2:10][CH2:11][C:6]2([C:2](=[O:1])[N:3]([C:16]3[CH:21]=[CH:20][C:19]([O:22][C:23]([F:26])([F:25])[F:24])=[CH:18][CH:17]=3)[CH2:4][CH2:5]2)[CH2:7][CH2:8]1)(=[O:14])=[O:13])[C:35]1[CH:30]=[CH:31][CH:32]=[CH:37][CH:36]=1Participants
3
Procedure
This material was prepared in analogy to example 285 step B) from 1-Oxo-2-(4-trifluoromethoxy-phenyl)-2,8-diaza-spiro[4.5]decane-8-sulfonyl chloride and ethyl-(2-pyridin-2-yl-ethyl)-amine. MS (ESI): 484.4 (MH+).
Sources & evidence
- ORD record
- ord-3139d91042234ef2b6a92a01927ab34d
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08329904B2
Reaction notes
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