Estrone → 3-Hydroxyestra-1,3,5(10)-triene-16,17-dione 16-oxime

HRID 11307

반응식

HRID 11307 반응식
CC(C)([O-])C.[K+].[K].[CH3:8][C@@:9]12[C:25](=[O:26])[CH2:24][CH2:23][C@H:22]1[C@H:21]1[C@@H:12]([C:13]3[CH:14]=[CH:15][C:16]([OH:27])=[CH:17][C:18]=3[CH2:19][CH2:20]1)[CH2:11][CH2:10]2.[N:28](OCCC(C)C)=[O:29]>C(O)(C)(C)C.O>[CH3:8][C@@:9]12[C:25](=[O:26])/[C:24](=[N:28]/[OH:29])/[CH2:23][C@H:22]1[C@@H:21]1[CH2:20][CH2:19][C:18]3[CH:17]=[C:16]([OH:27])[CH:15]=[CH:14][C:13]=3[C@H:12]1[CH2:11][CH2:10]2

참가 물질

7

반응물 4

HCID 5870EstroneHCID 8053Isoamyl NitriteHCID 5462222PotassiumHCID 23665647Potassium tert-butoxide

생성물 1

HCID 95617673-Hydroxyestra-1,3,5(10)-triene-16,17-dione 16-oxime

시약·촉매·용매 2

HCID 962Water용매HCID 6386tert-Butanol용매

실험 절차

To a stirred solution of potassium tert-butoxide under an atmosphere of N2, freshly prepared by dissolving potassium metal (80 mg, 2.05 mmol) in 2 mL tert-butanol, oestrone (200 mg, 740 mmol) was added. The reaction mixture was then stirred for 1 hour at room temperature under N2 and isoamyl nitrite (180 μmol, 1.34 mmol) was added dropwise. The deep red mixture obtained was stirred overnight and then poured into water (20 mL). The resulting solution was extracted with ether (2×20 mL) and the aqueous layer was acidified with glacial acetic acid. (10 mL) to give a light yellow precipitate. This was left separating for two hours after which the solid was filtered (140 mg, 63%): mp 223–225° C. (lit. 226–227° C.);43 TLC (chloroform/acetone, 9:1) Rf 0.27 cf. Rf 0.69 (E1); IR (KBr) 3385 (NOH), 2920–2860 (aliph CH), 1735 (C═O), 1605–1500 (arom C═C) cm−1; δH (DMSO-d6, 400 MHz) 0.89 (3H, s, C-18-H3), 1.30–2.85 (11H, m), 2.70–2.81 (2H, m, C-6-H2), 6.46 (1H, d, JC-2-H,C-4-H=2.3 Hz, C-4-H), 6.52 (1H, dd, JC-1-H,C-2-H=8.4 Hz and JC-4-H,C-2-H=2.3 Hz, C-2-H), 7.05 (1H, d, JC-2-H,C-1-H=8.2 Hz, C-1-H), 9.05 (1H, s, exchanged with D2O, OH) and 12.39 (1H, s, exchanged with D2O, NOH); δc (DMSO-d6, 100.4 MHz) 14.09 (q, C-18), 25.09 (t); 25.46 (t), 26.18 (t), 29.02 (t), 30.92 (t), 37.20 (d), 43.20 (d), 44.59 (d), 48.50 (s, C-13), 112.70 (d), 114.83 (d), 125.82 (d), 129.59 (s), 136.88. (s), 154.84 (s, C-3 or C-16), 155.23 (s, C-3 or C-16) and 204.64 (s, C═O); MS m/z (FAB+) 453.2 [30, (M+H+NBA)+], 300.1 [100, (M+H)+]; MS m/z (FAB−) 451.3 [38, (M−H+NBA)−], 298.2 [100, (M−H)−]; Acc MS m/z (FAB+) 300.15963, C18H22NO3 requires 300.115997. CHN,

후처리

  1. additionwas added
  2. customThe deep red mixture obtained
  3. stirringwas stirred overnight
  4. extractionThe resulting solution was extracted with ether (2×20 mL)
  5. custom(10 mL) to give a light yellow precipitate
  6. waitThis was left
  7. customseparating for two hours after which the solid
  8. filtrationwas filtered (140 mg, 63%)
  9. custommp 223–225° C. (lit. 226–227° C.);43 TLC (chloroform/acetone, 9:1) Rf 0.27

출처 및 근거

ORD 기록
ord-7423384ad4ba4b52b3db5009c5cdea3d
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07098218B2

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