Sulfuric Acid → 6-(4-chloro-2-pyridin-3-yl-benzyl)-9-hydroxy-2-isopropyl-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione

HRID 2169422노트

반응식

HRID 2169422 반응식
C([O:8][C:9]1[C:14](=[O:15])[N:13]=[C:12]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][C:18]=2[C:24]2[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=2)[N:11]2[CH2:30][CH2:31][N:32]([CH:35]([CH3:37])[CH3:36])[C:33](=[O:34])[C:10]=12)C1C=CC=CC=1.OS(O)(=O)=O>C(O)(=O)C>[Cl:23][C:20]1[CH:21]=[CH:22][C:17]([CH2:16][C:12]2[N:11]3[CH2:30][CH2:31][N:32]([CH:35]([CH3:37])[CH3:36])[C:33](=[O:34])[C:10]3=[C:9]([OH:8])[C:14](=[O:15])[N:13]=2)=[C:18]([C:24]2[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=2)[CH:19]=1

참가 물질

4

실험 절차

To a stirred solution of 9-benzyloxy-6-(4-chloro-2-pyridin-3-yl-benzyl)-2-isopropyl-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione (389) (45 mg, 0.088 mmol) in acetic acid (2 mL), concentrated H2SO4 (0.001 mL, 0.018 mmol) was added and the reaction mixture was stirred for 4 h at room temperature (monitored by LC-MS). From the reaction, volatiles were removed and the residue was quenched with ice col d water (5 mL). Aqueous saturated NaHCO3 was added to adjust the pH up to 8. The quenched mass was extracted with ethyl acetate (2×15 mL), the combined organic part was dried, concentrated and purified by preparative HPLC to get 6-(4-chloro-2-pyridin-3-yl-benzyl)-9-hydroxy-2-isopropyl-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione (390) (12.0 mg, 32.26%) as an off-white solid.

후처리

  1. customFrom the reaction, volatiles
  2. customwere removed
  3. customthe residue was quenched with ice col
  4. additionAqueous saturated NaHCO3 was added
  5. extractionThe quenched mass was extracted with ethyl acetate (2×15 mL)
  6. customthe combined organic part was dried
  7. concentrationconcentrated
  8. custompurified by preparative HPLC

출처 및 근거

ORD 기록
ord-19bc0da260ba4980a1c9034b64a03877
출처 데이터셋
uspto-grants-2015_06
특허 번호
US09045486B2

반응 노트

불러오는 중…