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Tris(1,1-dimethylethyl)phosphine → 1-(Tetrahydro-2H-pyran-4-yl)-1H-indol-5-amine

HRID 1668481
ノート
印刷プレビュー

反応式

HRID 1668481 の反応式
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1)[CH:6]=[CH:5]2.C(P(C(C)(C)C)C(C)(C)C)(C)(C)C.C[Si]([N-:34][Si](C)(C)C)(C)C.[Li+]>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].O1CCCC1>[O:14]1[CH2:15][CH2:16][CH:11]([N:7]2[C:8]3[C:4](=[CH:3][C:2]([NH2:34])=[CH:10][CH:9]=3)[CH:5]=[CH:6]2)[CH2:12][CH2:13]1
参加物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 83681Tris(1,1-dimethylethyl)phosphineHCID 2733832Lithium hexamethyldisilazaneHCID 590046455-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-indole

生成物 1

HCID 590046181-(Tetrahydro-2H-pyran-4-yl)-1H-indol-5-amine収率 88.8%

試薬・触媒・溶媒 2

HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Compound 88 (140 mg, 0.500 mmol), tris(dibenzylideneacetone)dipalladium (0) (45.7 mg, 0.050 mmol) and anhydrous tetrahydrofuran (15 mL) were charged to a dry argon purged flask fitted with magnetic stir bar and condenser. A solution of tri-tert-butylphosphine (10 wt % in hexane, 202.3 mg, 0.100 mmol) is added followed by dropwise addition of a 1M tetrahydrofuran solution of lithium bis(trimethylsilyl)amide (1.500 ml, 1.500 mmol) and mixture refluxed for a period of 45 minutes. The mixture was cooled to room temperature then to 0° C., quenched with 1M HCl (10 mL) and stirred for 15 minutes. The solution was diluted with ethyl acetate and conc. NH4OH added to adjust pH to 9. The mixture was transferred to a separatory funnel and the organic layer collected. The aqueous layer was further extracted with ethyl acetate and the combined organic layers were washed with brine, dried over magnesium sulphate, filtered, concentrated and the residue purified via chromatography on silica gel (EtOAc: Hexanes, 7:3) to yield a pale brown solid 89 (96 mg, 88.8%). 1H NMR (DMSO-d6) δ 1.80-1.99 (m, 4H), 3.53 (dt, 2H, J=11.4, 2.9 Hz), 3.95-3.99 (m, 2H), 4.39-4.50 (m, 1H), 4.55 (brs, 2H), 6.14 (d, 1H, J=4.1 Hz), 6.52 (dd, 1H, J=8.8, 2.1 Hz), 6.68 (d, 1H, J=1.9 Hz), 7.23 (d, 1H, J=8.6 Hz), 7.27 (d, 1H, J=3.2 Hz); ESI-MS (m/z, %): 217 (MH+, 100%).

後処理

  1. customfitted with magnetic stir bar and condenser
  2. temperaturerefluxed for a period of 45 minutes
  3. customto 0° C., quenched with 1M HCl (10 mL)
  4. additionThe solution was diluted with ethyl acetate and conc. NH4OH
  5. additionadded
  6. customThe mixture was transferred to a separatory funnel
  7. customthe organic layer collected
  8. extractionThe aqueous layer was further extracted with ethyl acetate
  9. washthe combined organic layers were washed with brine
  10. dry with materialdried over magnesium sulphate
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customthe residue purified via chromatography on silica gel (EtOAc: Hexanes, 7:3)

出典と根拠

ORDレコード
ord-5926c278447a4027886654218b123775
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07989447B2

反応ノート

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