2,2,6,6-Tetramethylpiperidine → 2-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)-1-(2-fluoro-5-neopentylpyridin-3-yl)ethanol

HRID 253140

反応式

HRID 253140 の反応式
CC1(C)CCCC(C)(C)N1.C([Li])CCC.[F:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[CH:19][N:18]=1.[Si:28]([O:35][C:36]1([CH2:40][CH:41]=[O:42])[CH2:39][CH2:38][CH2:37]1)([C:31]([CH3:34])([CH3:33])[CH3:32])([CH3:30])[CH3:29]>C1COCC1.O>[Si:28]([O:35][C:36]1([CH2:40][CH:41]([C:22]2[C:17]([F:16])=[N:18][CH:19]=[C:20]([CH2:23][C:24]([CH3:27])([CH3:26])[CH3:25])[CH:21]=2)[OH:42])[CH2:37][CH2:38][CH2:39]1)([C:31]([CH3:34])([CH3:33])[CH3:32])([CH3:30])[CH3:29]

参加物

7

反応物 4

HCID 130352,2,6,6-TetramethylpiperidineHCID 575158452-Fluoro-5-neopentylpyridineHCID 866140212-(1-((Tert-butyldimethylsilyl)oxy)cyclobutyl)acetaldehydeHCID 178418339Butyllithium

生成物 1

HCID 668448842-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)-1-(2-fluoro-5-neopentylpyridin-3-yl)ethanol

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-78 °C

実験手順

2,2,6,6-tetramethylpiperidine (13.0 ml, 76.5 mmol) was dissolved in 500 ml THF and cooled to −78° C. Butyllithium (26.8 ml, 67.0 mmol) was added over the period of 10 min and the reaction was allowed to warm up to 0° C. and kept there for 3 min. The mixture was cooled back to −78° C. and a solution of 2-fluoro-5-neopentylpyridine (8.000 g, 47.8 mmol) in 10 ml THF was added over the period of 30 min. The mixture was stirred for 20 min at the same temperature and a solution of 2-(1-(tert-butyldimethylsilyloxy)cyclobutyl) acetaldehyde (19.7 g, 86.1 mmol) in 25 ml THF was added over the period of 20 min. The reaction was stirred for 15 min at the same temperature and hydrolyzed with 200 ml of H2O. The mixture was allowed to warm up to room temp and extracted 2 times with 1 L EtOAc (each). The combined organic extracts were dried over MgSO4 and evaporated. The crude material was used without further purification. MS found 396.2.

後処理

  1. temperatureto warm up to 0° C.
  2. temperatureThe mixture was cooled back to −78° C.
  3. temperatureto warm up to room temp
  4. extractionextracted 2 times with 1 L EtOAc (each)
  5. dry with materialThe combined organic extracts were dried over MgSO4
  6. customevaporated
  7. customThe crude material was used without further purification

出典と根拠

ORDレコード
ord-83d78029e2c740839623dea869f94173
出典データセット
uspto-grants-2011_01
特許番号
US07872009B2

関連ノート

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