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Tributyltin Chloride → 7-(Pyridin-3-yl)carbonyl-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole

HRID 1072324
ノート
印刷プレビュー

反応式

HRID 1072324 の反応式
[CH2:1]([Sn:5](Cl)([CH2:10][CH2:11][CH2:12][CH3:13])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].C1COCC1.[N:30]1[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([C:38]2[N:39]=[CH:40][N:41]3[CH:45]=[CH:44][S:43][C:42]=23)=[O:37])[CH:31]=1.[Cl-].[NH4+]>C1COCC1>[N:30]1[CH:35]=[CH:34][CH:33]=[C:32]([C:36]([C:38]2[N:39]=[CH:40][N:41]3[CH:45]=[C:44]([Sn:5]([CH2:10][CH2:11][CH2:12][CH3:13])([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:1][CH2:2][CH2:3][CH3:4])[S:43][C:42]=23)=[O:37])[CH:31]=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

6

反応物 4

HCID 15096Tributyltin ChlorideHCID 25517Ammonium ChlorideHCID 223903557-(Pyridin-3-yl)carbonylimidazo[5,1-b]thiazoleHCID 23714775LiHMDS tetrahydrofuran3 回

生成物 1

HCID 223903847-(Pyridin-3-yl)carbonyl-2-(tri-n-butylstannyl)imidazo[5,1-b]thiazole

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-50 °C

実験手順

Tri-n-butylstannyl chloride (0.841 ml) and 2.95 ml of a 1.0 N lithium bis(trimethylsilyl)amide/THF solution were added to a solution of 520 mg of 7-(pyridin-3-yl)carbonylimidazo[5,1-b]thiazole in 25 ml of THF at −60° C. under an argon atmosphere, and the mixture was stirred for 20 min. The temperature of the mixture was raised to −50° C., 1.0 ml of a 1.0 N lithium bis(trimethylsilyl)amide/THF solution was added thereto, and the mixture was stirred for 30 min. The temperature of the mixture was raised to −40° C., 0.5 ml of a 1.0 N lithium bis(trimethylsilyl)amide/THF solution was added thereto, and the mixture was stirred for 30 min. An aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate, followed by washing with brine. The organic layer was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=2:1→ethyl acetate only) to give 712 mg of the title compound.

後処理

  1. stirringthe mixture was stirred for 30 min
  2. temperatureThe temperature of the mixture was raised to −40° C.
  3. stirringthe mixture was stirred for 30 min
  4. extractionthe mixture was extracted with ethyl acetate
  5. washby washing with brine
  6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  7. customThe solvent was then removed by distillation
  8. customthe residue was purified by column chromatography on silica gel (hexane

出典と根拠

ORDレコード
ord-2001be10c4314a4a95c5fde4c48fadd7
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06908913B2

反応ノート

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