Réaction #57458

Équation de réaction

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride

(2S)-4-amino-4-oxo-2-[(2-quinolinylcarbonyl)amino]butanoic acid hydrochloride

1-hydroxybenzotriazole hydrate

diisopropylethylamine

tert-butyl N-((1S,2R)-1-benzyl-3-(cyclohexyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate

→

(2S)-N1-((1S,2R)-1-benzyl-3-(cyclohexyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)-2-[(2-quinolinylcarbonyl)amino]butanediamide

Solvants

N,N-dimethylformamide

trifluoroacetic acid

Conditions de réaction

Traitement

1. 1
   AutreThe TFA was removed under vacuum
2. 2
   workup.DISSOLUTIONthe resulting residue was dissolved in ethyl acetate
3. 3
   Lavagewashed with 5% aq. potassium carbonate solution, brine
4. 4
   Séchagedried over magnesium sulfate
5. 5
   Concentrationconcentrated to a residue
6. 6
   Autrewere combined at room temperature
7. 7
   AutreThe crude reaction mixture
8. 8
   Concentrationwas concentrated to a residue
9. 9
   workup.DISSOLUTIONdissolved in ethyl acetate
10. 10
    Lavagewashed with 1N HCl, 5% aq. potassium carbonate solution, brine
11. 11
    Séchagedried over magnesium sulfate
12. 12
    ConcentrationThe solution was concentrated to a residue
13. 13
    Autrepurified by silica gel chromatography (ethyl acetate)
14. 14
    Autrelyophylized providing a fluffy white solid

Mode opératoire

tert-butyl N-((1S,2R)-1-benzyl-3-(cyclohexyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate (0.18 mmol, 100 mg) was stirred in 1 mL trifluoroacetic acid (TFA) at room temperature for 1 hour. The TFA was removed under vacuum, and the resulting residue was dissolved in ethyl acetate, washed with 5% aq. potassium carbonate solution, brine, dried over magnesium sulfate, and concentrated to a residue. The resulting free amine, (2S)-4-amino-4-oxo-2-[(2-quinolinylcarbonyl)amino]butanoic acid hydrochloride (0.18 mmol, 56 mg), 1-hydroxybenzotriazole hydrate (0.18 mmol, 25 mg), N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.20 mmol, 38 mg), diisopropylethylamine (0.91 mmol, 0.157 mL) and anhydrous N,N-dimethylformamide (0.5 mL) were combined at room temperature and stirred for 15 hours. The crude reaction mixture was concentrated to a residue, dissolved in ethyl acetate, washed with 1N HCl, 5% aq. potassium carbonate solution, brine and dried over magnesium sulfate. The solution was concentrated to a residue, purified by silica gel chromatography (ethyl acetate), and lyophylized providing a fluffy white solid. H-1-NMR (CDCl3): δ 9.19-9.17 (1H,m), 8.32-8.30 (1H,m), 8.23-8.16 (2H,m), 7.89-7.87 (1H,m), 7.79-7.76 (3H,m), 7.65-7.61 (1H,m), 7.13-7.11 (2H,m), 7.05-6.94 (6H,m), 5.73-5.64 (1H,m), 5.41-5.33 (1H,m), 4.96-4.85 (1H,m), 4.28-4.08 (2H,m), 3.89-3.74 (1H,m), 3.86 (3H,s), 3.25 (1H,bs), 2.95-2.79 (5H,m), 2.65-2.60 (1H,m), 2.04 (2H,bs), 1.70 (2H,bs), 1.57-1.41 (1H,m), 1.30-1.10 (5H,m); MS (ESI): M+H=719.

Source