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Cesium carbonate → HCID 67430540、化合物

HRID 1040141
ノート
印刷プレビュー

反応式

HRID 1040141 の反応式
Cl[C:2]1[N:7]=[C:6]([O:8][CH:9]2[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]2)[CH:5]=[CH:4][N:3]=1.[NH2:22][C:23]1[CH:24]=[C:25]([C:32]2[S:36][C:35]([C:37]3([OH:41])[CH2:40][CH2:39][CH2:38]3)=[N:34][CH:33]=2)[CH:26]=[C:27]([N+:29]([O-:31])=[O:30])[CH:28]=1.CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C(=O)([O-])[O-].[Cs+].[Cs+]>O1CCOCC1.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[OH:41][C:37]1([C:35]2[S:36][C:32]([C:25]3[CH:24]=[C:23]([NH:22][C:2]4[N:7]=[C:6]([O:8][CH:9]5[CH2:14][CH2:13][N:12]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:11][CH2:10]5)[CH:5]=[CH:4][N:3]=4)[CH:28]=[C:27]([N+:29]([O-:31])=[O:30])[CH:26]=3)=[CH:33][N:34]=2)[CH2:40][CH2:39][CH2:38]1
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

7

反応物 4

HCID 10796Cesium carbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 584562421-[5-(3-Amino-5-nitrophenyl)-1,3-thiazol-2-yl]cyclobutanolHCID 71629906tert-Butyl 4-((2-chloropyrimidin-4-yl)oxy)piperidine-1-carboxylate

生成物 1

HCID 67430540HCID 67430540、化合物収率 70.4%

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 312751,4-Dioxane溶媒

反応条件

温度
100 °C

実験手順

To the product from Step 1 (900 mg, 2.87 mmol) and Intermediate 22 (836 mg, 2.87 mmol) in dioxane (28 mL) was added palladium acetate (129 mg, 0.574 mmol), XantPhos (498 mg, 0.860 mmol) and cesium carbonate (1.87 g, 5.74 mmol). The mixture was degassed with Ar for 10 min and then heated at 100° C. for 20 h. After cooling to ambient temperature, the reaction mixture was filtered through celite and washed with ethyl acetate and methanol. After solvent removal, the residue was purified by column chromatography on silica gel (0-90%, ethyl acetate: 10:1 methanol in hexanes) to afford tert-butyl 4-{[2-({3-[2-(1-hydroxycyclobutyl)-1,3-thiazol-5-yl]-5-nitrophenyl}amino)pyrimidin-4-yl]oxy}piperidine-1-carboxylate (1.15 g, 2.02 mmol, 70%). MS ESI: [M+H]+ m/z 569.2.

後処理

  1. customThe mixture was degassed with Ar for 10 min
  2. temperatureAfter cooling to ambient temperature
  3. filtrationthe reaction mixture was filtered through celite
  4. washwashed with ethyl acetate and methanol
  5. customAfter solvent removal
  6. customthe residue was purified by column chromatography on silica gel (0-90%, ethyl acetate: 10:1 methanol in hexanes)

出典と根拠

ORDレコード
ord-02cb1acb94384bebb506a8830a56d2d7
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551984B2

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