Pyridine → HCID 10339998, 화합물

HRID 369044노트

반응식

HRID 369044 반응식
[CH3:1][O:2][C@H:3]1[CH2:20][C@@:18]2([CH3:19])[C@@H:14]([CH2:15][CH2:16][C:17]2=[O:21])[C@H:13]2[C@H:4]1[C:5]1[CH:6]=[CH:7][C:8]([OH:22])=[CH:9][C:10]=1[CH2:11][CH2:12]2.C1(C)C=CC(S(O)(=O)=[O:30])=CC=1.N1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>C1(C)C=CC=CC=1.O1CCCC1.O1C=CCCC1.C(OCC)(=O)C>[CH3:1][O:2][C@H:3]1[CH2:20][C@@:18]2([CH3:19])[C@@H:14]([CH2:15][CH2:16][C:17]2=[O:21])[C@H:13]2[C@H:4]1[C:5]1[CH:6]=[CH:7][C:8]([O:22][CH:39]3[CH2:38][CH2:37][CH2:36][CH2:35][O:30]3)=[CH:9][C:10]=1[CH2:11][CH2:12]2

참가 물질

8

실험 절차

A suspension of 2.0 g of 11β-methoxy-3-hydroxy-estra-1,3,5(10)-trien-17-one in 20 ml of toluene, 5 ml of tetrahydrofuran and 3.0 ml of dihydropyran is stirred with 20 mg of para-toluenesulfonic acid for 24 hours at room temperature. Then, 0.5 ml of pyridine is added, diluted with ethyl acetate, washed with sodium bicarbonate solution as well as with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/acetone. 1.9 g of 11β-methoxy-3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one is obtained as crystals with a melting point of 147° C., [α]D22 =+147.2° (c=0.5% in pyridine).

후처리

  1. washwashed with sodium bicarbonate solution as well as with saturated sodium chloride solution
  2. customdried on sodium sulfate
  3. concentrationconcentrated by evaporation in a vacuum
  4. customchromatographed on silica gel with hexane/acetone

출처 및 근거

ORD 기록
ord-4ffee451002a49b6b1e6c0d866b76534
출처 데이터셋
uspto-grants-2000_10
특허 번호
US06136800

반응 노트

불러오는 중…