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Tert-Butyl nitrite → HCID 58687906、化合物

HRID 1988572
ノート
印刷プレビュー

反応式

HRID 1988572 の反応式
N[C:2]1[CH:15]=[C:14]2[C:5]([S:6][C:7]3[C:8]([C:16]4[O:17][C:18]([N:23]5[CH2:28][CH2:27][O:26][CH2:25][CH2:24]5)=[CH:19][C:20](=[O:22])[CH:21]=4)=[CH:9][CH:10]=[CH:11][C:12]=3[CH2:13]2)=[CH:4][CH:3]=1.F[B-](F)(F)F.[H+].N([O:37][C:38](C)(C)C)=O.C([SiH](C(C)C)C(C)C)(C)C>C(O)C.C(OCC)C.CC([O-])=O.CC([O-])=O.[Pd+2]>[N:23]1([C:18]2[O:17][C:16]([C:8]3[CH:9]=[CH:10][CH:11]=[C:12]4[C:7]=3[S:6][C:5]3[CH:4]=[CH:3][C:2]([CH:38]=[O:37])=[CH:15][C:14]=3[CH2:13]4)=[CH:21][C:20](=[O:22])[CH:19]=2)[CH2:28][CH2:27][O:26][CH2:25][CH2:24]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

8

反応物 4

HCID 10906Tert-Butyl nitriteHCID 28118Tetrafluoroboric acidHCID 138754Silane, tris(1-methylethyl)-HCID 221394022-(7-Amino-9H-thioxanthen-4-yl)-6-morpholin-4-yl-pyran-4-one

生成物 1

HCID 58687906HCID 58687906、化合物収率 76.1%

試薬・触媒・溶媒 3

HCID 167845
palladium(II) acetate
触媒
HCID 702Ethanol溶媒
HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

To a suspension of 2-(7-amino-9H-thioxanthen-4-yl)-6-morpholin-4-yl-pyran-4-one (1)(0.50 g, 1.27 mmol) in ethanol (4 mL) at room temperature was added tetrafluorboric acid (supplied as 54 wt % in diethyl ether, 0.35 mL, 2.54 mmol). The solution was then cooled to 0° C., when t-butyl nitrite (750 μL, 6.33 mmol) was added. After 1 hr, the reaction was diluted with diethyl ether (10 mL), and after 20 mins the precipitate was filtered and washed with diethyl ether. The orange coloured salt was then dissolved in MeCN:Et2O (1:1) (15 mL), when triisopropylsilane (222 mg, 1.40 mmol) and Pd(OAc)2 (5.47 g, 24.37 mmol) were added successively. A CO pressure of 10 atm was then applied for 10 minutes, after which the reaction was filtered. The organic layer was washed with saturated NaHCO3 then brine, dried over MgSO4, filtered and concentrated in vacuo. The resulting yellow/orange solid was dried under vacuum at 50° C. to give the crude title compound (0.392 g, 75%, 2 steps) which was used without any further purification. m/z (LC-MS, ESP), RT=3.40 min, (M++1)=406.3

後処理

  1. filtrationafter 20 mins the precipitate was filtered
  2. washwashed with diethyl ether
  3. dissolutionThe orange coloured salt was then dissolved in MeCN:Et2O (1:1) (15 mL)
  4. filtrationafter which the reaction was filtered
  5. washThe organic layer was washed with saturated NaHCO3
  6. dry with materialbrine, dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe resulting yellow/orange solid was dried under vacuum at 50° C.

出典と根拠

ORDレコード
ord-7638747ed6cc4c6db45e3af79dcaf7df
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07642254B2

反応ノート

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