Sodium hydride → 5-(3-Cyclohexyl-propoxy)-1-(4-nitro-phenyl)-1H-tetrazole

HRID 1071180노트

반응식

HRID 1071180 반응식
[CH:1]1([CH2:7][CH2:8][CH2:9][OH:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Na+].Cl[C:14]1[N:18]([C:19]2[CH:24]=[CH:23][C:22]([N+:25]([O-:27])=[O:26])=[CH:21][CH:20]=2)[N:17]=[N:16][N:15]=1>O1CCCC1>[CH:1]1([CH2:7][CH2:8][CH2:9][O:10][C:14]2[N:18]([C:19]3[CH:20]=[CH:21][C:22]([N+:25]([O-:27])=[O:26])=[CH:23][CH:24]=3)[N:17]=[N:16][N:15]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

참가 물질

5

실험 절차

Cyclohexylpropyl alcohol (237 mL, 1.56 mol) was added to a suspension of NaH (66.0 g, 1.65 mol) in tetrahydrofuran (1.40 L). A solution of 5-Chloro-1-(4-nitro-phenyl)-1H-tetrazole (320 g, 1.42 mol) in tetrahydrofuran (900 mL) was added dropwise over 1.5 hours. The reaction was allowed to cool to room temperature and stirred overnight. The mixture was concentrated in vacuo to a solid. The solid was dissolved in ethyl acetate, washed with saturated aqueous sodium chloride solution (2×), dried (Na2SO4), and filtered through silica gel (700 g). The red filtrate was concentrated in vacuo until product began to precipitate from solution. Hexane was added and the slurry filtered to provide a tan solid (320 g, 64%). Mp 82-88° C. (dec); 1H NMR (CDCl3, 300 MHz) δ 8.43 (d, 9.2 Hz, 2H), 8.04 (d, 9.2 Hz, 2H), 4.70 (t, 7.0 Hz, 2H), 1.96 (m, 2H), 1.75-1.64 (m, 5H), 1.39-1.13 (m, 6H), 0.97-0.87 (m, 2H); MS (CI) m/z 332 (MH+); Anal. calcd for C16H21N5O3: C, 57.99; H, 6.39; N, 21.13. Found: C, 57.80; H, 6.35; N, 21.02; Rf=0.43 (N).

후처리

  1. concentrationThe mixture was concentrated in vacuo to a solid
  2. dissolutionThe solid was dissolved in ethyl acetate
  3. washwashed with saturated aqueous sodium chloride solution (2×)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered through silica gel (700 g)
  6. concentrationThe red filtrate was concentrated in vacuo until product
  7. customto precipitate from solution
  8. additionHexane was added
  9. filtrationthe slurry filtered

출처 및 근거

ORD 기록
ord-b10ad2b68e2e47c1826cbfdc33a87c5c
출처 데이터셋
uspto-grants-2005_06
특허 번호
US06903218B2

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