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2,6-Lutidine → 7-[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazol-3-yl]-2-(4-methoxy-benzyl)-5-methyl-2H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one

HRID 1907146
ノート
印刷プレビュー

反応式

HRID 1907146 の反応式
[NH2:1][C:2]1[C:3]([CH3:23])=[CH:4][C:5]2[C:9]([C:10]=1[C:11]([OH:13])=[O:12])=[N:8][N:7]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)[CH:6]=2.[Cl:24][C:25]1[C:26]([N:31]2[C:35]([C:36](O)=O)=[CH:34][C:33]([O:39][CH3:40])=[N:32]2)=[N:27][CH:28]=[CH:29][CH:30]=1.C(Cl)(=O)C(Cl)=O.N1C(C)=CC=CC=1C.CS(Cl)(=O)=O>C(#N)C>[Cl:24][C:25]1[C:26]([N:31]2[C:35]([C:36]3[O:12][C:11](=[O:13])[C:10]4[C:9]5=[N:8][N:7]([CH2:14][C:15]6[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=6)[CH:6]=[C:5]5[CH:4]=[C:3]([CH3:23])[C:2]=4[N:1]=3)=[CH:34][C:33]([O:39][CH3:40])=[N:32]2)=[N:27][CH:28]=[CH:29][CH:30]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 79372,6-LutidineHCID 31297Methanesulfonyl chlorideHCID 65578Oxalyl chlorideHCID 509892861-(3-chloropyridin-2-yl)-3-methoxy-1H-pyrazole-5-carboxylic acidHCID 585004296-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid

生成物 1

HCID 58500462
7-[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazol-3-yl]-2-(4-methoxy-benzyl)-5-methyl-2H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A suspension of 6-amino-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid (0.288 g, 0.925 mmol) in acetonitrile (4 ml) was stirred at 20° C. for 10 minutes before the acyl chloride prepared from 2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazole-3-carboxylic acid and oxalyl chloride (0.265 g, 0.971 mmol) was added. After 45 minutes stirring, 2,6-lutidine (0.215 ml) was added, followed 10 minutes later by methanesulfonyl chloride (0.072 ml, 0.925 mmol). After 18 hours of reaction, the mixture was concentrated under vacuum and water (25 ml) was added. The product was extracted with ethyl acetate and purified by flash chromatography on silica gel using a gradient from 50% to 100% ethyl acetate in cyclohexane. The desired product was obtained as light orange crystals.

後処理

  1. additionwas added
  2. customAfter 18 hours of reaction
  3. concentrationthe mixture was concentrated under vacuum and water (25 ml)
  4. additionwas added
  5. extractionThe product was extracted with ethyl acetate
  6. custompurified by flash chromatography on silica gel using a gradient from 50% to 100% ethyl acetate in cyclohexane

出典と根拠

ORDレコード
ord-ea766e1c642f40588e83d01e65061c7f
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08598078B2

反応ノート

読み込み中…

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