(Z)-Prop-1-en-1-ylboronic acid → HCID 178439564, 화합물

HRID 1019715

반응식

HRID 1019715 반응식
Br[C:2]1[N:7]=[C:6]2[N:8]([C@H:12]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH3:13])[C:9]([OH:11])=[N:10][C:5]2=[N:4][CH:3]=1.[CH:20](/B(O)O)=[CH:21]/[CH3:22]>>[C:14]1([C@@H:12]([N:8]2[C:6]3=[N:7][C:2](/[CH:20]=[CH:21]\[CH3:22])=[CH:3][N:4]=[C:5]3[N:10]=[C:9]2[OH:11])[CH3:13])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

참가 물질

3

반응 조건

온도
90 °C

실험 절차

A scintillation vial equipped with a stirbar was charged with (S)-6-bromo-1-(1-phenylethyl)-1H-imidazo[4,5-b]pyrazin-2-ol (1.0 equiv), (Z)-prop-1-enyl boronic acid (2.0 equiv) and (DPPF)PdCl2 (0.10 equiv). The vial was fitted with a septum-lined cap and purged with nitrogen for 5-10 min. To this mixture was added dioxane (16.6 volume equivalents) and degassed 2N K2CO3 (4.2 volume equivalents) by syringe. The resulting mixture was heated to 90° C. overnight. The mixture was cooled to room temperature, diluted with EtOAc, washed with twice with saturated aq. NaHCO3, and once with brine. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Biotage MPLC 5%-40% EtOAc/Hexanes) provided the title compound (63%) as an off-white foam. LCMS m/z (APCI)=281.1 (M+H).

후처리

  1. customA scintillation vial equipped with a stirbar
  2. customThe vial was fitted with a septum-lined
  3. customcap
  4. custompurged with nitrogen for 5-10 min
  5. additionTo this mixture was added dioxane (16.6 volume equivalents)
  6. customdegassed 2N K2CO3 (4.2 volume equivalents) by syringe
  7. temperatureThe mixture was cooled to room temperature
  8. additiondiluted with EtOAc
  9. washwashed with twice with saturated aq. NaHCO3
  10. dry with materialThe organic layer was dried over sodium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-cada75ad2ad64e5fae809388d65267b8
출처 데이터셋
uspto-grants-2014_05
특허 번호
US08716291B2

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