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Potassium Carbonate → Hydrochloric Acid

HRID 912014
ノート
印刷プレビュー

反応式

HRID 912014 の反応式
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([N:14]2[CH:18]=[C:17](B3OC(C)(C)C(C)(C)O3)[CH:16]=[N:15]2)[CH2:10][CH2:9]1)=O)(C)(C)C.Br[C:29]1[C:33]2[CH:34]=[N:35][C:36]([NH2:50])=[C:37]([O:38][CH:39]([C:41]3[C:46]([Cl:47])=[CH:45][CH:44]=[C:43]([F:48])[C:42]=3[Cl:49])[CH3:40])[C:32]=2[O:31][CH:30]=1.C(=O)([O-])[O-].[K+].[K+]>COCCOC.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:49][C:42]1[C:43]([F:48])=[CH:44][CH:45]=[C:46]([Cl:47])[C:41]=1[CH:39]([O:38][C:37]1[C:32]2[O:31][CH:30]=[C:29]([C:17]3[CH:16]=[N:15][N:14]([CH:11]4[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]4)[CH:18]=3)[C:33]=2[CH:34]=[N:35][C:36]=1[NH2:50])[CH3:40].[ClH:47]
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

8

反応物 3

HCID 11430Potassium CarbonateHCID 45480279tert-butyl 4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylateHCID 674022843-Bromo-7-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]furo[3,2-c]pyridin-6-ylamine

生成物 2

HCID 313Hydrochloric AcidHCID 578124837-[1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-3-(1-piperidin-4-yl-1H-pyrazol-4-yl)-furo[3,2-c]pyridin-6-ylamine

試薬・触媒・溶媒 3

HCID 178418397HCID 178418397、化合物触媒HCID 962Water溶媒HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
100 °C

実験手順

To a stirred mixture of 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (26.94 mg, 0.071 mmol), 3-bromo-7-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]furo[3,2-c]pyridin-6-ylamine (20.0 mg, 0.047 mmol), potassium carbonate (19.7 mg, 0.14 mmol) in DME (2.0 mL) and H2O (0.40 mL) was added Pd(PPh3)4 (2.8 mg, 0.0024 mmol) under Nitrogen. The resulting mixture was refluxed at 100° C. for 30 min. LC-MS indicated completion of reaction. The solvent was then removed under reduced pressure and the resulting residue was purified by a flash chromatography (2% MeOH in DCM). MS (ES+): m/z 590.07, 592.08 (MH+). HPLC: tR=3.48 min (ZQ3, polar—5 min). The product purified above was then dissolved in 2 mL dioxane, to this solution was added solution of 4 N HCl in dioxane (1 mL) at r.t., the resulting mixture was stirred at r.t. for 1.5 h. LC-MS indicated completion of reaction. The solvent was removed under reduced pressure to give the title compound as HCl salt. The 1H NMR spectrum matches that of Example 5.

後処理

  1. customcompletion of reaction
  2. customThe solvent was then removed under reduced pressure
  3. customthe resulting residue was purified by a flash chromatography (2% MeOH in DCM)
  4. custom5 min
  5. customThe product purified above
  6. dissolutionwas then dissolved in 2 mL dioxane, to this solution
  7. additionwas added solution of 4 N HCl in dioxane (1 mL) at r.t.
  8. customcompletion of reaction
  9. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-e37e9154ed2f4b948cfd02b8cc6ea934
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08022206B2

反応ノート

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