Isopropanol → (1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR 13bR)-benzyl 9-(4-(methoxycarbonyl)phenyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate

HRID 406880

반응식

HRID 406880 반응식
[CH3:1][C@:2]12[C@@:19]3([CH3:20])[C@@H:10]([C@:11]4([CH3:31])[C@@H:16]([CH2:17][CH2:18]3)[C:15]([CH3:22])([CH3:21])[C:14](OS(C(F)(F)F)(=O)=O)=[CH:13][CH2:12]4)[CH2:9][CH2:8][CH:7]1[C@H:6]1[C@H:32]([C:35]([CH3:37])=[CH2:36])[CH2:33][CH2:34][C@:5]1([C:38]([O:40][CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)=[O:39])[CH2:4][CH2:3]2.CC(O)C.O.C(=O)([O-])[O-].[Na+].[Na+].[CH3:59][O:60][C:61]([C:63]1[CH:68]=[CH:67][C:66](B(O)O)=[CH:65][CH:64]=1)=[O:62]>O1CCOCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[CH3:59][O:60][C:61]([C:63]1[CH:68]=[CH:67][C:66]([C:14]2[C:15]([CH3:22])([CH3:21])[C@H:16]3[C@:11]([CH3:31])([CH2:12][CH:13]=2)[C@@H:10]2[C@:19]([CH3:20])([C@@:2]4([CH3:1])[C@H:7]([CH2:8][CH2:9]2)[C@H:6]2[C@H:32]([C:35]([CH3:37])=[CH2:36])[CH2:33][CH2:34][C@:5]2([C:38]([O:40][CH2:41][C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=2)=[O:39])[CH2:4][CH2:3]4)[CH2:18][CH2:17]3)=[CH:65][CH:64]=1)=[O:62]

참가 물질

8

반응물 4

HCID 3776IsopropanolHCID 27343694-Methoxycarbonylphenylboronic acidHCID 2735133Sodium Carbonate MonohydrateHCID 88415331(1R,3aS,5aR,5bR,7aR,11aR,11bR,13bR)-benzyl 5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-9-(trifluoromethylsulfonyloxy)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate

생성물 1

HCID 67776728(1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR 13bR)-benzyl 9-(4-(methoxycarbonyl)phenyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate수율 68.4%

시약·촉매·용매 3

HCID 178418397HCID 178418397, 화합물촉매HCID 962Water용매HCID 312751,4-Dioxane용매

실험 절차

To a round bottom flask containing a solution of (1R,3aS,5aR,5bR,7aR,11aR,11bR,13bR)-benzyl 5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-9-(trifluoromethylsulfonyloxy)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate (6.21 g, 9.18 mmol) in dioxane (25 mL) was added 2-propanol (25 mL) and water (15 mL) followed by sodium carbonate monohydrate (3.42 g, 27.5 mmol), 4-methoxycarbonylphenylboronic acid (2.478 g, 13.77 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.318 g, 0.275 mmol). The flask was attached to a reflux condenser, was flushed with N2, and was heated to reflux overnight. After heating the mixture for 14.5 h, it was cooled to rt and was diluted with water (75 mL). The mixture was extracted with ethyl acetate (3×75 mL) and washed with brine. The combined organic layers were dried with MgSO4, filtered, and concentrated under reduced pressure. The residue was adsorbed to silica gel and was purified by Biotage flash chromatography using a 0-20% EtOAc in hexanes gradient. The fractions containing the expected product was combined and concentrated under reduced pressure. The expected product, (1R,3aS,5aR,5bR,7aR,11aS,11bR,13aR 13bR)-benzyl 9-(4-(methoxycarbonyl)phenyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-2,3,3a,4,5,5a,5b,6,7,7a,8,11,11a,11b,12,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysene-3a-carboxylate (4.16 g, 6.28 mmol, 68.4% yield), was isolated as a white foam. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 0.82 (s, 3H), 0.87-1.75 (m, 17H), 0.91 (s, 3H), 0.92 (s, 3H), 0.95 (s, 3H), 0.97 (s, 3H), 1.69 (s, 3H), 1.82-1.95 (m, 2H), 2.09 (dd, J=17.24, 6.26 Hz, 1H), 2.20-2.32 (m, 2H), 3.04 (td, J=10.91, 4.73 Hz, 1H), 3.90 (s, 3H), 4.60 (s, 1H), 4.73 (d, J=1.83 Hz, 1H), 5.07-5.19 (m, 2H), 5.28 (dd, J=6.10, 1.83 Hz, 1H), 7.19 (d, J=8.24 Hz, 2H), 7.29-7.40 (m, 5H), 7.92 (d, J=8.24 Hz, 2H).

후처리

  1. customThe flask was attached to a reflux condenser
  2. customwas flushed with N2
  3. temperaturewas heated
  4. temperatureto reflux overnight
  5. temperatureAfter heating the mixture for 14.5 h
  6. additionwas diluted with water (75 mL)
  7. extractionThe mixture was extracted with ethyl acetate (3×75 mL)
  8. washwashed with brine
  9. dry with materialThe combined organic layers were dried with MgSO4
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure
  12. customwas purified by Biotage flash chromatography
  13. additionThe fractions containing the expected product
  14. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-5cec97e01766494caad652be36614696
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08754068B2

연결된 노트

불러오는 중…