N-Allylpyridin-3-amine → (S)-3-Amino-1-(pyridin-3-yl)azepan-2-one trifluoroacetate
Reaction equation
[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[NH2:8][C@H:9]1[CH2:15][CH2:14][CH2:13][CH2:12][N:11]([C:16]2[CH:21]=[CH:20][CH:19]=C[C:17]=2OC)[C:10]1=[O:24].C([NH:28]C1C=NC=CC=1)C=C>>[F:1][C:2]([F:7])([F:6])[C:3]([OH:5])=[O:4].[NH2:8][C@H:9]1[CH2:15][CH2:14][CH2:13][CH2:12][N:11]([C:16]2[CH:17]=[N:28][CH:19]=[CH:20][CH:21]=2)[C:10]1=[O:24]Participants
3
Procedure
(S)-3-Amino-1-(pyridin-3-yl)azepan-2-one trifluoroacetate (36 mg, 0.11 mmol) was synthesized as described for the preparation of Intermediate 62 using N-allylpyridin-3-amine in step A. Anal. Calcd. for C11H15N3O m/z 205.2. found: 206.1 (M+H)+.
Sources & evidence
- ORD record
- ord-664d4fa16ffd4c6994b4271ab4b9fd07
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346852B2
Reaction notes
Loading…