反応 #1994330

ord-903aaf3de9c84d15a539f4a521fd51da

反応方程式

Cc1cc(O)cc(C)c1C[C@H](N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1
(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-[(R)-1-(3-phenyl-propylcarbamoyl)-ethyl]-propionamide
Cc1cc(C)n(C(=N)N)n1
3,5-dimethylpyrazole-1-carboxamidine
CCN(CC)CC
triethylamine
Cc1cc(O)cc(C)c1C[C@H](NC(=N)N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1
title compound
Cc1cc(O)cc(C)c1C[C@H](NC(=N)N)C(=O)N[C@H](C)C(=O)NCCCc1ccccc1
(S)-2-Guanidino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-[(R)-1-(3-phenyl-propylcarbamoyl)-ethyl]-propionamide
N
NH3

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction was heated for a further 24 hours
  2. 2
    その他The solvent was evaporated
  3. 3
    workup.DISSOLUTIONthe crude material was redissolved in dichloromethane containing 2% methanol
  4. 4
    洗浄The resulting solution was washed with a solution of citric acid
  5. 5
    洗浄The organic phase was washed with brine
  6. 6
    乾燥then dried over MgSO4
  7. 7
    ろ過The organics were filtered
  8. 8
    その他evaporated
  9. 9
    その他leaving a small amount of a crude gum
  10. 10
    その他The gum was purified
  11. 11
    洗浄elution from 95:5:0.5 to 80:20:5 DCM

実験手順

(S)-2-Amino-3-(4-hydroxy-2,6-dimethyl-phenyl)-N-[(R)-1-(3-phenyl-propylcarbamoyl)-ethyl]-propionamide (J. Med. Chem. 1994, 37, 888) (449 mg, 1.0 mmol) and 3,5-dimethylpyrazole-1-carboxamidine (240 mg, 1.2 mmol) were heated in ethanol at 60° C. After 24 hours, triethylamine (167 μl, 1.2 mmol) was added. The reaction was heated for a further 24 hours. The solvent was evaporated and the crude material was redissolved in dichloromethane containing 2% methanol. The resulting solution was washed with a solution of citric acid followed by sodium bicarbonate solution. The organic phase was washed with brine then dried over MgSO4. The organics were filtered and evaporated leaving a small amount of a crude gum. The gum was purified using an ISCO chromatography system on a 12 g silica column using gradient elution from 95:5:0.5 to 80:20:5 DCM:MeOH:NH3 to afford the title compound as a solid in 5% yield, 20 mg. 1H NMR (400 MHz, MeOH-d4) δ : 1.18 (d, 3H), 1.75-1.82 (m, 2H), 2.21 (s, 1H), 2.49 (s, 1H), 2.58-2.63 (m, 2H), 2.95-3.02 (m, 1H), 3.10-3.24 (m, 3H), 3.28-3.32 (m, 1H), 4.18-4.22 (m, 1H), 4.35-4.40 (m, 1H), 6.51 (s, 2H), 7.08-7.28 (m, 5H). LRMS m/z 440 [M+H]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08598123B2uspto-grants-2013_12