Iodine → 4-Iodophenylalanine

HRID 1664106ノート

反応式

HRID 1664106 の反応式
[NH2:1][C@@H:2]([CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.II.[I:20]([O-])(=O)=O.[Na+]>C(O)(=O)C>[NH2:1][C@@H:2]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([I:20])=[CH:9][CH:8]=1)[C:3]([OH:5])=[O:4]

参加物

6

反応条件

温度
70 °C

実験手順

To a solution (S)-2-amino-3-phenylpropanoic acid 91 (4.01 g, 24.3 mmol) in acetic acid (22 mL) was added sulfuric acid (2.9 mL, 5.14 mmol), iodine (2.47 g, 4.7 mmol) and sodium iodate (1.02 g, 5.14 mmol). The mixture was heated to 70° C. and allowed to stir at this temperature for 16 h before an additional portion of sodium iodate (1.02 g, 5.14 mmol) was added. The reaction was left for a further 2 h before being concentrated, dissolved in methanol (20 mL) and treated with NaOH (60 mL). The mixture was left to precipitate out of the basic solution overnight and the resulting solid was filtered by vacuum filtration to yield the title compound (7.07 g, 24.3 mmol, 100%) as a pink solid, which had spectral data in agreement with that reported.93 [α]D21 −10.6 (c. 0.3, HCl). Mp 258-260° C. (lit. 261-262° C.)93 1H NMR (CD3OD, 300 MHz): δ 7.71 (d, J=8.4 Hz, 2H, ArH2′ and ArH6′); 7.10 (d, J=8.4 Hz, 2H, ArH3′ and ArH5′); 4.26 (dd, J=6.3, 7.2 Hz, H2); 3.26 (dd, J=5.4, 14.1 Hz, 1H, H3a); 3.04 (dd, J=7.2, 14.4 Hz, 1H, H3b). Mass Spectrum (CI, +ve) m/z 279 (100%), 292 (70%) [M+]. HRMS calcd for C9H11NO2 291.9834 found 291.9568.

後処理

  1. additionwas added
  2. concentrationbefore being concentrated
  3. dissolutiondissolved in methanol (20 mL)
  4. additiontreated with NaOH (60 mL)
  5. waitThe mixture was left
  6. customto precipitate out of the basic solution overnight
  7. filtrationthe resulting solid was filtered by vacuum filtration

出典と根拠

ORDレコード
ord-c05abed2e1e145ec95b5d1ca45889eb6
出典データセット
uspto-grants-2011_10
特許番号
US08039430B2

反応ノート

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