Diisopropylethylamine → HCID 76282616, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[N:11]=[C:10]([C:12]([OH:14])=O)[CH:9]=[CH:8][C:7]=2[N:15]2[CH2:18][C:17]([F:20])([F:19])[CH2:16]2)[CH2:3][CH2:2]1.[C:21]([NH:25][CH2:26][CH2:27][C:28]([NH2:30])=[O:29])([CH3:24])([CH3:23])[CH3:22].CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.CCN(C(C)C)C(C)C>>[C:21]([N:25]([CH2:26][CH2:27][C:28](=[O:29])[NH2:30])[C:12]([C:10]1[CH:9]=[CH:8][C:7]([N:15]2[CH2:18][C:17]([F:20])([F:19])[CH2:16]2)=[C:6]([O:5][CH2:4][CH:1]2[CH2:2][CH2:3]2)[N:11]=1)=[O:14])([CH3:24])([CH3:23])[CH3:22]Participants
5
Procedure
In analogy to the procedure described in Example 47 b), 6-cyclopropylmethoxy-5-(3,3-difluoro-azetidin-1-yl)-pyridine-2-carboxylic acid (Example 1 b)) was reacted with 3-(tert-butylamino)propanamide (289656-97-9) in the presence of TBTU and DIEA to obtain the title compound as colorless oil; MS (EI): m/e=411.6 [MH+].
Sources & evidence
- ORD record
- ord-30b3b084acbe415394767280a432f9c5
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09303012B2
Reaction notes
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