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

Water → HCID 22048236、化合物

HRID 1833135
ノート
印刷プレビュー

反応式

HRID 1833135 の反応式
P(Cl)(Cl)(Cl)=O.C(OC([N:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][C:15]([O:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[C:16]([O:21][CH3:22])[CH:17]=2)[CH:12]1[CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[C:34]([O:38][CH3:39])[CH:33]=1)=O)C.O.[OH-].[K+].CN(C)[CH:45]=[O:46]>CO.ClCCl>[CH2:24]([O:23][C:15]1[CH:14]=[C:13]2[C:18]([C:19]([CH:45]=[O:46])=[CH:20][N:11]=[C:12]2[CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[C:34]([O:38][CH3:39])[CH:33]=2)=[CH:17][C:16]=1[O:21][CH3:22])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 962Water2 回HCID 6228Dimethylformamide2 回HCID 14797Potassium HydroxideHCID 24813Phosphorus oxychlorideHCID 21034936HCID 21034936、化合物

生成物 1

HCID 22048236HCID 22048236、化合物収率 53%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回
HCID 6344Dichloromethane溶媒

実験手順

To N,N-dimethylformamide (0.36 mL) at 0° C. was added phosphorous oxychloride (0.84 mL, 0.80 g, 10.9 mmol.) dropwise. The mixture was warmed to room temperature and stirred×30 minutes. The mixture was recooled in an ice-bath, and 7-benzyloxy-6-methoxy-1-(3-methoxy-benzyl)-1H-isoquinoline-2-carboxylic acid ethyl ester (2.15 g, 2.11 mmol) in N,N-dimethylformamide (5 mL) was added dropwise. After addition was complete, the mixture was heated on an oil bath×2 hours at 60° C. The mixture was cooled, poured into water (50 mL) and extracted with ethyl acetate (3×20 mL). The combined organic extracts were washed with water (3×20 mL), saturated aqueous sodium chloride solution (1×20 mL) and dried over anhydrous magnesium sulfate. Concentration of the solvent in vacuo gave a viscous oil that was dissolved methanol (20 mL), and a solution of powdered potassium hydroxide (0.63 g, 10.5 mmol) in methanol (5 mL) was added dropwise. The mixture was stirred overnight (14 hours) at room temperature. The mixture was poured into water (100 mL) and extracted with diethyl ether (3×30 mL). The combined organic extracts were washed with water (30 mL), saturated aqueous sodium chloride solution (30 mL) and dried over anhydrous magnesium sulfate. Concentration gave an orange foam that was dissolved in dichloromethane (100 mL), and maganese (IV) oxide (3 g, 34.8 mmol.) was added in one portion. The mixture was stirred at room temperature×2 hours. Silica gel (5 g) was added to the mixture. The mixture was filtered through a silica gel pad. The silica gel pad was washed with 50% ethyl acetate in hexanes (200 mL). Concentration of the combined filtrates and precipitation from ethyl acetate with hexanes gave 7-benzyloxy-6-methoxy-1-(3-methoxy-benzyl)-isoquinoline-4-carbaldehyde (1.00 g, 2.42 mmol, 53%) as a yellow solid.

後処理

  1. customThe mixture was recooled in an ice-bath
  2. additionAfter addition
  3. temperaturethe mixture was heated on an oil bath×2 hours at 60° C
  4. temperatureThe mixture was cooled
  5. extractionextracted with ethyl acetate (3×20 mL)
  6. washThe combined organic extracts were washed with water (3×20 mL), saturated aqueous sodium chloride solution (1×20 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customConcentration of the solvent in vacuo gave a viscous oil that
  9. stirringThe mixture was stirred overnight (14 hours) at room temperature
  10. extractionextracted with diethyl ether (3×30 mL)
  11. washThe combined organic extracts were washed with water (30 mL), saturated aqueous sodium chloride solution (30 mL)
  12. dry with materialdried over anhydrous magnesium sulfate
  13. concentrationConcentration
  14. customgave an orange foam that
  15. stirringThe mixture was stirred at room temperature×2 hours
  16. additionSilica gel (5 g) was added to the mixture
  17. filtrationThe mixture was filtered through a silica gel pad
  18. washThe silica gel pad was washed with 50% ethyl acetate in hexanes (200 mL)
  19. customConcentration of the combined filtrates and precipitation from ethyl acetate with hexanes

出典と根拠

ORDレコード
ord-34eeffa6c3174a94a051168a352cd588
出典データセット
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07067529B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート