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Methanesulfonic Acid → 5-Methyl-N-{5-methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-yl}-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxamide mesylate

HRID 1748624
ノート
印刷プレビュー

反応式

HRID 1748624 の反応式
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:4]=[CH:5][C:6]([N:9]2[C:13]([CH3:14])=[C:12]([C:15]([NH2:17])=[O:16])[CH:11]=[N:10]2)=[N:7][CH:8]=1.[N:20]1([CH:26]2[CH2:31][CH2:30][C:29]([C:32]3[C:37]([CH3:38])=[CH:36][C:35](Br)=[CH:34][N:33]=3)=[CH:28][CH2:27]2)[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1.C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:46][S:47]([OH:50])(=[O:49])=[O:48]>O1CCOCC1.C(Cl)(Cl)Cl.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C2C=CC=CC=2)C2C3OC4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C(C)(C)C=3C=CC=2)C=CC=CC=1>[S:47]([OH:50])(=[O:49])(=[O:48])[CH3:46].[CH3:14][C:13]1[N:9]([C:6]2[CH:5]=[CH:4][C:3]([C:2]([F:1])([F:18])[F:19])=[CH:8][N:7]=2)[N:10]=[CH:11][C:12]=1[C:15]([NH:17][C:35]1[CH:34]=[N:33][C:32]([C:29]2[CH2:30][CH2:31][CH:26]([N:20]3[CH2:21][CH2:22][O:23][CH2:24][CH2:25]3)[CH2:27][CH:28]=2)=[C:37]([CH3:38])[CH:36]=1)=[O:16]
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

9

反応物 4

HCID 6395Methanesulfonic AcidHCID 10796Cesium carbonateHCID 471413721-(5-trifluoromethylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxamideHCID 866924794-[4-(5-Bromo-3-methylpyridin-2-yl)cyclohex-3-en-1-yl]morpholine

生成物 1

HCID 866925665-Methyl-N-{5-methyl-6-[4-(morpholin-4-yl)cyclohex-1-en-1-yl]pyridin-3-yl}-1-[5-(trifluoromethyl)pyridin-2-yl]-1H-pyrazole-4-carboxamide mesylate

試薬・触媒・溶媒 4

HCID 167845palladium(II) acetate触媒HCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)触媒HCID 6212Chloroform溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

A suspension of 1-(5-trifluoromethylpyridin-2-yl)-5-methyl-1H-pyrazole-4-carboxamide (2.2 g) described in Reference Example 120, 2-(4-(morpholin-4-yl)cyclohex-1-en-1-yl)-3-methyl-5-bromopyridine (2.75 g) described in Reference Example 107, 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (152 mg), palladium acetate (39 mg) and cesium carbonate (4.01 g) in 1,4-dioxane (30 ml) was stirred at 100° C. After the reaction, the reaction solution was left stand, ice water was added and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate, and concentrated. The resulting residue was purified with a silica gel column chromatography (chloroform/methanol), washed with ethanol and the resulting solid was filtered and dried at 60° C. in vacuo to give a white solid. Methanesulfonic acid (0.326 ml) was added to a solution of the resulting solid in chloroform (200 ml) and stirred at room temperature for three hours. Then, the solvent was evaporated, ethanol was added and the precipitated solid was filtered and dried at 60° C. in vacuo to give the titled compound (2.9 g) as a white solid.

後処理

  1. customAfter the reaction
  2. additionwas added
  3. extractionextracted with chloroform
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe resulting residue was purified with a silica gel column chromatography (chloroform/methanol)
  7. washwashed with ethanol
  8. filtrationthe resulting solid was filtered
  9. customdried at 60° C. in vacuo
  10. customto give a white solid
  11. stirringstirred at room temperature for three hours
  12. customThen, the solvent was evaporated
  13. additionethanol was added
  14. filtrationthe precipitated solid was filtered
  15. customdried at 60° C. in vacuo

出典と根拠

ORDレコード
ord-432cc8a7aeb34fa7a66a54e5136bf816
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150555B2

反応ノート

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