Dimethylformamide → (S)-2-amino-2-(3-fluoro-5-iodophenyl)ethyl di-tert-butyl phosphate

HRID 596042ノート

反応式

HRID 596042 の反応式
[C:1]([O:5][P:6]([O:13][CH2:14][C@@H:15]([NH:24]C(=O)OCC1C2C=CC=CC=2C2C1=CC=CC=2)[C:16]1[CH:21]=[C:20]([I:22])[CH:19]=[C:18]([F:23])[CH:17]=1)([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7])([CH3:4])([CH3:3])[CH3:2].CN(C=O)C.N1CCCCC1.C(N1CCCCC1)(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O>C(OCC)(=O)C>[P:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])([O:5][C:1]([CH3:2])([CH3:4])[CH3:3])([O:13][CH2:14][C@@H:15]([NH2:24])[C:16]1[CH:21]=[C:20]([I:22])[CH:19]=[C:18]([F:23])[CH:17]=1)=[O:7]

参加物

6

実験手順

To (S)-(9H-fluoren-9-yl)methyl (2-((di-tert-butoxyphosphoryl)oxy)-1-(3-fluoro-5-iodophenyl)ethyl)carbamate (6450 mg, 9.27 mmol) was added DMF (Volume: 90 mL) followed by piperidine (25 mL, 253 mmol) and stirred at room temperature for 30 minutes, followed by LCMS. To the crude reaction mixture was added 750 ml of ethyl acetate, washed with saturated sodium bicarbonate (2×), water (5×), saturated salt solution, dried sodium sulfate, and filtered. The solvent was concentrated off to constant mass under high vacuum to give the desire crude product which includes FMOC piperidine impurity, used as is. LCMS (m/z): 474.2 (MH+), 0.80 min.

後処理

  1. customTo the crude reaction mixture
  2. washwashed with saturated sodium bicarbonate (2×), water (5×), saturated salt solution, dried sodium sulfate
  3. filtrationfiltered
  4. concentrationThe solvent was concentrated off to constant mass under high vacuum
  5. customto give the desire crude product which
  6. custom474.2 (MH+), 0.80 min.

出典と根拠

ORDレコード
ord-19e6287ad4b94eaaa8dc70079e006e6c
出典データセット
uspto-grants-2016_01
特許番号
US09242996B2

反応ノート

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