Tetrabutylammonium Fluoride → HCID 86669236, 화합물

HRID 2366860노트

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HRID 2366860 반응식
[C:1]([N:4]1[C:13]2[C:8](=[CH:9][C:10]([C:14]#[C:15][Si](C)(C)C)=[CH:11][CH:12]=2)[C@H:7]([NH:20][C:21](=[O:26])[O:22][CH:23]([CH3:25])[CH3:24])[CH2:6][C@@H:5]1[CH3:27])(=[O:3])[CH3:2].CCCC[N+](CCCC)(CCCC)CCCC.[F-]>O1CCCC1>[CH3:25][CH:23]([O:22][C:21](=[O:26])[NH:20][C@H:7]1[C:8]2[C:13](=[CH:12][CH:11]=[C:10]([C:14]#[CH:15])[CH:9]=2)[N:4]([C:1](=[O:3])[CH3:2])[C@@H:5]([CH3:27])[CH2:6]1)[CH3:24]

참가 물질

4

실험 절차

To a solution of 1-methylethyl {(2S,4R)-1-acetyl-2-methyl-6-[(trimethylsilyl)ethynyl]-1,2,3,4-tetrahydro-4-quinolinyl}carbamate (for a preparation, see Intermediate 59) (216 mg, 0.559 mmol) in tetrahydrofuran (THF) (3 mL) at room temperature was added TBAF (1M in THF, 0.671 mL, 0.671 mmol) and the resulting black mixture was stirred at this temperature for 35 min. Most of the solvent was removed in vacuo and the residue dissolved in AcOEt. The organic phase was washed with a saturated NaHCO3 aqueous solution then twice with brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue on SP4 using a 10 G silica cartridge (Gradient: 13 to 63% AcOEt in Hexanes) gave 1-methylethyl[(2S,4R)-1-acetyl-6-ethynyl-2-methyl-1,2,3,4-tetrahydro-4-quinolinyl]carbamate (156 mg, 0.496 mmol, 89% yield) as a very pale yellow foam.

후처리

  1. customat room temperature
  2. customMost of the solvent was removed in vacuo
  3. dissolutionthe residue dissolved in AcOEt
  4. washThe organic phase was washed with a saturated NaHCO3 aqueous solution
  5. dry with materialtwice with brine, dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customPurification of the residue on SP4

출처 및 근거

ORD 기록
ord-3cbc084630874d619ab31ba8b6c970fd
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08697725B2

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