Pyridine → HCID 10339998、化合物

HRID 850828ノート

反応式

HRID 850828 の反応式
[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

参加物

8

反応物 3

HCID 1049PyridineHCID 6101p-Toluenesulfonic acidHCID 1120881311beta-Methoxy-3-hydroxy-estra-1,3,5(10)-trien-17-one

生成物 1

HCID 10339998HCID 10339998、化合物

試薬・触媒・溶媒 4

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒HCID 80803,4-dihydro-2H-pyran溶媒HCID 8857Ethyl Acetate溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-d42a695279444eb592a0df2f429b74fc
出典データセット
uspto-grants-2000_01
特許番号
US06018062

反応ノート

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