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Iodo benzene diacetate → 8-(Tert-butyldimethylsilyloxy)-2-(6-fluoro[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinoline

HRID 876439
ノート
印刷プレビュー

反応式

HRID 876439 の反応式
[Si:1]([O:8][C:9]1[CH:10]=[CH:11][CH:12]=[C:13]2[C:18]=1[N:17]=[C:16]([CH:19]=O)[CH:15]=[CH:14]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[F:21][C:22]1[CH:23]=[CH:24][C:25]([NH:28][NH2:29])=[N:26][CH:27]=1.C(O)(=O)C.C(O)(=O)C.IC1C=CC=CC=1>O.C(Cl)Cl>[Si:1]([O:8][C:9]1[CH:10]=[CH:11][CH:12]=[C:13]2[C:18]=1[N:17]=[C:16]([C:19]1[N:26]3[CH:27]=[C:22]([F:21])[CH:23]=[CH:24][C:25]3=[N:28][N:29]=1)[CH:15]=[CH:14]2)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
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

6

反応物 3

HCID 12217721Iodo benzene diacetate2 回HCID 199167865-Fluoro-2-hydrazinylpyridineHCID 585670828-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde

生成物 1

HCID 672311328-(Tert-butyldimethylsilyloxy)-2-(6-fluoro[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinoline収率 57%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

8-(tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde (1.39 g, 4.83 mmol) and 5-fluoro-2-hydrazinylpyridine (1.28 g, 6.04 mmol) were combined in DCM (12.1 mL, 4.83 mmol) at ambient temperature and stirred for 15 minutes. The mixture was cooled to 0° C. followed by addition of iodobenzene diacetate (IBD; 1.87 g, 5.80 mmol). The reaction was warmed to ambient temperature and stirred overnight. Additional IBD (0.8 equivalents, 4.64 mmol) was added and the reaction was allowed to stir at ambient temperature for 48 hours total. The mixture was transferred to a separatory funnel, diluting with water and DCM. The organic phase was washed with saturated aqueous Na2SO3, followed by back extraction of the aqueous phase 2 times with DCM. The organics were combined and washed with brine, dried over Na2SO4, filtered and concentrated to a residue under reduced pressure, followed by purification by flash column chromatography to give the product (1.08 g, 57% yield). MS APCI (+) m/z 395.3 (M+1) detected.

後処理

  1. temperatureThe reaction was warmed to ambient temperature
  2. stirringstirred overnight
  3. stirringto stir at ambient temperature for 48 hours total
  4. customThe mixture was transferred to a separatory funnel
  5. washThe organic phase was washed with saturated aqueous Na2SO3
  6. extractionfollowed by back extraction of the aqueous phase 2 times with DCM
  7. washwashed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated to a residue under reduced pressure
  11. customfollowed by purification by flash column chromatography

出典と根拠

ORDレコード
ord-2b7e935582a74667b14622e10f3e2dc7
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987251B2

反応ノート

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