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Sodium Bicarbonate → HCID 67338716、化合物

HRID 1668959
ノート
印刷プレビュー

反応式

HRID 1668959 の反応式
I[C:2]1[C:11]([CH3:12])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][N:6]=[C:7]2[NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=1.[CH3:24][N:25]1[C:30]2[N:31]=[C:32]([NH:35][CH3:36])[N:33]=[CH:34][C:29]=2[CH:28]=[C:27](B2OC(C)(C)C(C)(C)O2)[C:26]1=[O:46].O.C(=O)([O-])[O-].[Na+].[Na+].C(=O)(O)[O-].[Na+]>CCOC(C)=O.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O.CN(C=O)C>[CH3:24][N:25]1[C:30]2[N:31]=[C:32]([NH:35][CH3:36])[N:33]=[CH:34][C:29]=2[CH:28]=[C:27]([C:2]2[C:11]([CH3:12])=[CH:10][CH:9]=[C:8]3[C:3]=2[CH:4]=[CH:5][N:6]=[C:7]3[NH:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=2)[C:26]1=[O:46]
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 516892Sodium BicarbonateHCID 2735133Sodium Carbonate MonohydrateHCID 58466448HCID 58466448、化合物HCID 673385755-iodo-6-methyl-N-(3-(trifluoromethyl)phenyl)isoquinolin-1-amine

生成物 1

HCID 67338716HCID 67338716、化合物収率 19.8%

試薬・触媒・溶媒 4

HCID 178418476
HCID 178418476、化合物
触媒
HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
160 °C

実験手順

To a solution of 5-iodo-6-methyl-N-(3-(trifluoromethyl)phenyl)isoquinolin-1-amine (0.1680 g, 0.392 mmol) in 10:1 DMF:Water (1.5 ml), charged to a 5 mL microwave reaction vessel, 8-methyl-2-(methylamino)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrido[2,3-d]pyrimidin-7(8H)-one (0.149 g, 0.471 mmol), dichlorobis(triphenyl-phosphine)palladium (ii) (0.0110 g, 0.0157 mmol), and sodium carbonate hydrate (0.102 g, 0.824 mmol) were added. The reaction mixture was stirred at 160° C. for 20 min. The reaction mixture was diluted with EtOAc and partioned with saturated sodium bicarbonate. The aqueous layer was extracted twice with EtOAc. The combined organics were washed with brine, dried over magnesium sulfate and concentrated under vacuum. The resulting residue was loaded on to silica and purified by silica gel chromatography (ISCO 2×12.0 g, 0-6% MeOH in DCM, 45 min.) and HPLC to give 8-methyl-6-(6-methyl-1-(3-(trifluoromethyl)phenylamino)isoquinolin-5-yl)-2-(methylamino)pyrido[2,3-d]pyrimidin-7(8H)-one (0.0381 g, 19.8% yield). MS (M+H)+ 491.

後処理

  1. extractionThe aqueous layer was extracted twice with EtOAc
  2. washThe combined organics were washed with brine
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated under vacuum
  5. custompurified by silica gel chromatography (ISCO 2×12.0 g, 0-6% MeOH in DCM, 45 min.) and HPLC

出典と根拠

ORDレコード
ord-c665eb1075484174a0a79b6793f6531e
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989461B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート