ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Potassium Hydroxide → (3S)-1-(6-methoxypyridin-2-yl)pyrrolidin-3-ol

HRID 338553
ノート
印刷プレビュー

反応式

HRID 338553 の反応式
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[N:3]=1.[NH:10]1[CH2:14][CH2:13][C@H:12]([OH:15])[CH2:11]1.[OH-].[K+]>O1CCCC1.CO.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].CC(P(C(C)(C)C)C1N(C2C(C3C=CC=CC=3)=NN(C3C=CC=CC=3)C=2C2C=CC=CC=2)N=CC=1)(C)C>[CH3:9][O:8][C:4]1[N:3]=[C:2]([N:10]2[CH2:14][CH2:13][C@H:12]([OH:15])[CH2:11]2)[CH:7]=[CH:6][CH:5]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 14797Potassium HydroxideHCID 870092-Chloro-6-methoxypyridineHCID 2733874(3S)-pyrrolidin-3-ol

生成物 1

HCID 86698868(3S)-1-(6-methoxypyridin-2-yl)pyrrolidin-3-ol収率 226.5%

試薬・触媒・溶媒 3

HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 11547931
BippyPhos
触媒
HCID 21899815MeOH tetrahydrofuran溶媒

反応条件

温度
70 °C

実験手順

To a solution of 2-chloro-6-methoxypyridine (1.966 g, 3.750 mmol) and commercially available (3S)-pyrrolidin-3-ol (1.437 g, 16.50 mmol) in tetrahydrofuran/methanol (137 mL/6.7 mL), was added Pd2(dba)3 (62.2 mg, 0.0688 mmol), BippyPhos (139.2 mg, 0.2750 mmol) and potassium hydroxide (1.16 g, 20.6 mmol, 88% pellets). The reaction was then was purged with nitrogen for 2 minutes and stirred at 70° C. for 18 hours. The reaction was filtered, quenched with saturated ammonium chloride solution, adjusted to pH=7˜8 with 1N hydrochloric acid and extracted with dichloromethane (100 mL*2) and ethyl acetate (100 mL*3). The combined organic phase was washed with saturated brine, dried over sodium sulfate and evaporated in vacuo. The residue was then purified by silica gel chromatography with ethyl acetate/petroleum ether, 0-25% to give the title compound (1.65 g, 62%) as a yellow gum that was used without further purification.

後処理

  1. customThe reaction was then was purged with nitrogen for 2 minutes
  2. filtrationThe reaction was filtered
  3. customquenched with saturated ammonium chloride solution
  4. extractionextracted with dichloromethane (100 mL*2) and ethyl acetate (100 mL*3)
  5. washThe combined organic phase was washed with saturated brine
  6. dry with materialdried over sodium sulfate
  7. customevaporated in vacuo
  8. customThe residue was then purified by silica gel chromatography with ethyl acetate/petroleum ether, 0-25%

出典と根拠

ORDレコード
ord-72e6bcacd29247ffb74c40060173fe7c
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889730B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート