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Morpholine → 1-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [1-(6-morpholin-4-yl-pyridin-3-yl)-cyclopropyl]-amide

HRID 2172981
ノート
印刷プレビュー

反応式

HRID 2172981 の反応式
Br[C:2]1[N:7]=[CH:6][C:5]([C:8]2([NH:11][C:12]([C:14]3[C:15]4[CH:22]=[N:21][N:20]([C:23]5[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=5)[C:16]=4[CH:17]=[N:18][CH:19]=3)=[O:13])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[NH:30]1[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1>CS(C)=O.CCOC(C)=O>[N:30]1([C:2]2[N:7]=[CH:6][C:5]([C:8]3([NH:11][C:12]([C:14]4[C:15]5[CH:22]=[N:21][N:20]([C:23]6[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=6)[C:16]=5[CH:17]=[N:18][CH:19]=4)=[O:13])[CH2:10][CH2:9]3)=[CH:4][CH:3]=2)[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 8083MorpholineHCID 529167991-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [1-(6-bromo-pyridin-3-yl)-cyclopropyl]-amide

生成物 1

HCID 529175031-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [1-(6-morpholin-4-yl-pyridin-3-yl)-cyclopropyl]-amide

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 8857Ethyl Acetate
溶媒

実験手順

A solution of 1-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [1-(6-bromo-pyridin-3-yl)-cyclopropyl]-amide (35 mg, 0.077 mmol) and morpholine (68 μL, 0.77 mmol) in DMSO (1 mL) is heated in a pressure tube at 160° C. After 40 hours, the mixture is cooled to room temperature, diluted with EtOAc (50 mL) and washed with saturated aqueous ammonium chloride (2×50 mL), saturated aqueous sodium bicarbonate (50 mL), brine (50 mL), dried over MgSO4, filtered and concentrated. The resulting solid is purified by silica gel chromatography eluting with a gradient of 0-5% methanol in dichloromethane to give a solid, which is triturated with ether (5 mL), filtered and dried to afford the title compound.

後処理

  1. washwashed with saturated aqueous ammonium chloride (2×50 mL), saturated aqueous sodium bicarbonate (50 mL), brine (50 mL)
  2. dry with materialdried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe resulting solid is purified by silica gel chromatography
  6. washeluting with a gradient of 0-5% methanol in dichloromethane
  7. customto give a solid, which
  8. customis triturated with ether (5 mL)
  9. filtrationfiltered
  10. customdried

出典と根拠

ORDレコード
ord-8daae4d9bdc645339ec1d543b611e020
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09056858B2

反応ノート

読み込み中…

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