2,6-Dichloropyrazine → HCID 86679156, compound
Reaction equation
[NH2:1][C@H:2]([CH:5]([CH3:7])[CH3:6])[CH2:3][OH:4].[Cl:8][C:9]1[CH:14]=[N:13][CH:12]=[C:11](Cl)[N:10]=1>>[Cl:8][C:9]1[N:10]=[C:11]([NH:1][C@H:2]([CH:5]([CH3:7])[CH3:6])[CH2:3][OH:4])[CH:12]=[N:13][CH:14]=1Participants
3
Procedure
In analogy to the procedures described for the preparation of intermediate A-20 and A-3 [C]: i) (R)-2-amino-3-methyl-butan-1-ol has been reacted with 2,6-dichloropyrazine to give (R)-2-(6-chloro-pyrazin-2-ylamino)-3-methyl-butan-1-ol; ii) subsequent condensation with 1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (intermediate A-1) gave the title compound as a light yellow solid. MS: 341.2 (M+H+).
Workup
- customIn analogy to the procedures described for the preparation of intermediate A-20 and A-3 [C]
Sources & evidence
- ORD record
- ord-3a19df59896e4e82b9cf6cf82f97a704
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09260408B2
Reaction notes
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