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Hexane → (4S,6S)-4-(2-fluoro-5-(6-((trimethylsilyl)ethynyl)pyridin-3-yl)phenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine

HRID 930325
ノート
印刷プレビュー

反応式

HRID 930325 の反応式
P([O-])([O-])([O-])=O.[K+].[K+].[K+].[F:9][C:10]1[CH:15]=[CH:14][C:13](B2OC(C)(C)C(C)(C)O2)=[CH:12][C:11]=1[C@:25]1([CH2:36][F:37])[CH2:30][C@@H:29]([C:31]([F:34])([F:33])[F:32])[O:28][C:27]([NH2:35])=[N:26]1.Br[C:39]1[CH:40]=[CH:41][C:42]([C:45]#[C:46][Si:47]([CH3:50])([CH3:49])[CH3:48])=[N:43][CH:44]=1.CCCCCC>O1CCOCC1.O.O.C(C1C(C(C)(C)C)=C([Pd]Cl)C=CC=1NC)(C)(C)C>[F:9][C:10]1[CH:15]=[CH:14][C:13]([C:39]2[CH:44]=[N:43][C:42]([C:45]#[C:46][Si:47]([CH3:48])([CH3:50])[CH3:49])=[CH:41][CH:40]=2)=[CH:12][C:11]=1[C@:25]1([CH2:36][F:37])[CH2:30][C@@H:29]([C:31]([F:33])([F:32])[F:34])[O:28][C:27]([NH2:35])=[N:26]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 8058HexaneHCID 62657Potassium Phosphate, TribasicHCID 109995845-Bromo-2-[2-(trimethylsilyl)ethynyl]pyridineHCID 86732145(4S,6S)-4-(2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine

生成物 1

HCID 86732153
(4S,6S)-4-(2-fluoro-5-(6-((trimethylsilyl)ethynyl)pyridin-3-yl)phenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine
収率 44.3%

試薬・触媒・溶媒 3

HCID 178482226HCID 178482226、化合物触媒HCID 962Water溶媒HCID 218864351,4-Dioxane--water (1/1)溶媒

実験手順

A mixture of potassium phosphate (0.676 g, 3.19 mmol), (4S,6S)-4-(2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (8b, 1.428 g, 3.40 mmol), 5-bromo-2-((trimethylsilyl)ethynyl)pyridine (0.270 g, 1.062 mmol) and 1,1-bis[(di-t-butyl-p-methylaminophenyl]palladium(II) chloride (0.038 g, 0.053 mmol) in dioxane/water (5.0/1.2 mL) was heated in microwave reactor at 110° C. for 35 min. The reaction mixture was diluted with water and extracted with DCM three times. The combined organic layers were washed with brine, dried on sodium sulfate, filtered and concentrated. The crude material was purified by silica gel chromatography: 0-100% EtOAc/hexane in 15 min. The product was obtained as an off-white solid. Trituration with hexane afforded the pure product as a white solid (0.22 g, 44% yield). MS m/z=468 [M+H]+. Calculated for C22H22F5N3OSi: 467.5.

後処理

  1. extractionextracted with DCM three times
  2. washThe combined organic layers were washed with brine
  3. customdried on sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified by silica gel chromatography
  7. customThe product was obtained as an off-white solid

出典と根拠

ORDレコード
ord-ded940f4a1494d38a1b5cccb9afe27b6
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09296734B2

反応ノート

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