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N,N-Dimethylglycine → 3-[4-amino-5-(2-benzyl-2H-indazol-6-yl)pyrrolo[2,1-f][1,2,4]triazin-7-yl]-1-(N,N-dimethylglycyl)piperidin-3-ol

HRID 1972925
ノート
印刷プレビュー

反応式

HRID 1972925 の反応式
[NH2:1][C:2]1[C:7]2=[C:8]([C:18]3[CH:19]=[CH:20][C:21]4[C:25]([CH:26]=3)=[N:24][N:23]([CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH:22]=4)[CH:9]=[C:10]([C:11]3([OH:17])[CH2:16][CH2:15][CH2:14][NH:13][CH2:12]3)[N:6]2[N:5]=[CH:4][N:3]=1.[CH3:34][N:35]([CH3:40])[CH2:36][C:37](O)=[O:38].CCN=C=NCCCN(C)C.Cl.C1C=CC2N(O)N=NC=2C=1.C(N(CC)C(C)C)(C)C>CN(C=O)C>[NH2:1][C:2]1[C:7]2=[C:8]([C:18]3[CH:19]=[CH:20][C:21]4[C:25]([CH:26]=3)=[N:24][N:23]([CH2:27][C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[CH:22]=4)[CH:9]=[C:10]([C:11]3([OH:17])[CH2:16][CH2:15][CH2:14][N:13]([C:37](=[O:38])[CH2:36][N:35]([CH3:40])[CH3:34])[CH2:12]3)[N:6]2[N:5]=[CH:4][N:3]=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 673N,N-DimethylglycineHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 585294413-[4-amino-5-(2-benzyl-2H-indazol-6-yl)pyrrolo[2,1-f][1,2,4]triazin-7-yl]piperidin-3-ol

生成物 1

HCID 58529359
3-[4-amino-5-(2-benzyl-2H-indazol-6-yl)pyrrolo[2,1-f][1,2,4]triazin-7-yl]-1-(N,N-dimethylglycyl)piperidin-3-ol
収率 33.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 3-[4-amino-5-(2-benzyl-2H-indazol-6-yl)pyrrolo[2,1-f][1,2,4]triazin-7-yl]piperidin-3-ol (154 mg, 0.35 mmol), N,N-dimethylglycine (43 mg, 0.42 mmol), EDCl (74 mg, 0.39 mmol), HOBt (52 mg, 0.39 mmol), and N,N-diisopropylethylamine (183 μL, 1.05 mmol) in DMF (3.0 mL) was stirred at rt for 80 h. The crude mixture was purified by preparative HPLC using a gradient elution from 15% to 45% acetonitrile in water followed by filtration through an acidic resin, washing with MeOH. The product was eluted with 2M NH3 in MeOH and the filtrate was concentrated to provide 61 mg (33%) of the desired product. ES-MS m/z 525.52 [M+H]+, HPLC RT (min) 2.04.

後処理

  1. customThe crude mixture was purified by preparative HPLC
  2. washa gradient elution from 15% to 45% acetonitrile in water
  3. filtrationfollowed by filtration through an acidic resin
  4. washwashing with MeOH
  5. washThe product was eluted with 2M NH3 in MeOH
  6. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-5be83b8f33f940f2b705f5a148bbbd7a
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08431695B2

反応ノート

読み込み中…

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