Methanol → 6-tert-Butyl-2-(2-hydroxymethyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-phenyl)-3,4-dihydro-2H-isoquinolin-1-one

HRID 2245697노트

반응식

HRID 2245697 반응식
[C:1]([C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[N:10]([C:16]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27]3[CH:32]=[C:31]([NH:33][C:34]4[CH:39]=[CH:38][C:37]([C:40]([N:42]5[CH2:47][CH2:46][O:45][CH2:44][CH2:43]5)=[O:41])=[CH:36][N:35]=4)[C:30](=[O:48])[N:29]([CH3:49])[CH:28]=3)[C:17]=1[CH2:18][O:19]C(=O)C)[CH2:9][CH2:8]2)([CH3:4])([CH3:3])[CH3:2].CO.O.O.[OH-].[Li+]>C1COCC1>[C:1]([C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][CH:14]=1)[C:11](=[O:15])[N:10]([C:16]1[CH:26]=[CH:25][CH:24]=[C:23]([C:27]3[CH:32]=[C:31]([NH:33][C:34]4[CH:39]=[CH:38][C:37]([C:40]([N:42]5[CH2:43][CH2:44][O:45][CH2:46][CH2:47]5)=[O:41])=[CH:36][N:35]=4)[C:30](=[O:48])[N:29]([CH3:49])[CH:28]=3)[C:17]=1[CH2:18][OH:19])[CH2:9][CH2:8]2)([CH3:4])([CH3:2])[CH3:3]

참가 물질

6

반응물 4

HCID 887Methanol2회HCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 59216446Acetic Acid 2-(6-tert-butyl-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-6-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-benzyl Ester

생성물 1

HCID 445467746-tert-Butyl-2-(2-hydroxymethyl-3-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-phenyl)-3,4-dihydro-2H-isoquinolin-1-one수율 33.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Acetic acid 2-(6-tert-butyl-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-6-{1-methyl-5-[5-(morpholine-4-carbonyl)-pyridin-2-ylamino]-6-oxo-1,6-dihydro-pyridin-3-yl}-benzyl ester (0.472 mmol) was taken up in THF (7 mL) and methanol (3 mL) and water (5 mL) and then added lithium hydroxide monohydrate (40 mg, 2 eq). The resulting mixture was stirred at room temperature overnight. The next morning the reaction was complete by TLC and most of the THF and methanol was removed under reduced pressure at 55° C. Then ethyl acetate (75 mL) and water (30 mL) were added and the layers were partitioned and then separated. Next, the ethyl acetate layer was washed with water (2×30 mL), brine (1×30 mL) and then dried over magnesium sulfate, filtered and concentrated to give 286 mg of crude product. Preparative Thin Layer Chromatography purification eluting on two 20×40 cm 1000 μM plates in 6% methanol in dicholomethane afforded the title compound (99 mg) as a white powder ((M+H)+=622).

후처리

  1. customwas removed under reduced pressure at 55° C
  2. additionThen ethyl acetate (75 mL) and water (30 mL) were added
  3. customthe layers were partitioned
  4. customseparated
  5. washNext, the ethyl acetate layer was washed with water (2×30 mL), brine (1×30 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give 286 mg of crude product
  10. customPreparative Thin Layer Chromatography purification
  11. washeluting on two 20×40 cm 1000 μM plates in 6% methanol in dicholomethane

출처 및 근거

ORD 기록
ord-7b3b9fd941e14af7b5dc701a0b8a9d33
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07683064B2

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