반응 #1810

반응 방정식

EDC

HCl.H2N-Gly-Asp(OBn)-Phe-OBn

diisopropylethylamine

dimethylformamide

HOBT

→

3-[6-Amino-2-pyridinyl]-propionyl-glycyl-(L)-aspartyl-(L)-phenylalanine

수율 10.0%

용매

ethanol

반응 조건

후처리

1. 1
   온도to warm to room temperature
2. 2
   기타the dimethylformamide was removed on a rotovap at 40° C
3. 3
   기타The residue was partitioned between ethyl acetate and water
4. 4
   세척the organic layer rinsed one time with water, two times with 5% citric acid
5. 5
   기타The organic solution was dried on sodium sulfate
6. 6
   기타the ethyl acetate removed
7. 7
   기타From this solution was recovered 85 mg (55%) of the starting peptide
8. 8
   추출extracted with dichloromethane
9. 9
   기타thus obtained on silica gel using 5% methanol/methylene chloride
10. 10
    기타The product thus obtained (30 mg, 0.5 mmol)
11. 11
    기타The flask was flushed with H2
12. 12
    workup.ADDITIONso an additional 7 mg of 10% Pd/C was added
13. 13
    기타After 24 additional hours, the solvents were removed
14. 14
    기타a roto-evaporator
15. 15
    workup.ADDITIONthe residue treated with 1% acetic acid in water
16. 16
    여과The solution was filtered
17. 17
    기타purified

실험 절차

3-(2-[6-Aminopyridyl])-propionic acid (63 mg, 0.28 mmol), HOBT (50 mg, 0.37 mmol), HCl.H2N-Gly-Asp(OBn)-Phe-OBn (155 mg, 0.28 mmol) and diisopropylethylamine were combined in 7 ml of dry dimethylformamide. The reaction mixture was cooled to 0° C. EDC (68 mg, 0.35 mmol) was added in one portion, the reaction mixture allowed to warm to room temperature and placed under argon. After 18 hours, the dimethylformamide was removed on a rotovap at 40° C. The residue was partitioned between ethyl acetate and water, and the organic layer rinsed one time with water, two times with 5% citric acid, once again with water, twice with 5% sodium bicarbonate solution, again with water, and finally one time with brine. The organic solution was dried on sodium sulfate, and the ethyl acetate removed. From this solution was recovered 85 mg (55%) of the starting peptide. The combined aqueous rinses were adjusted to pH 9 using dilute NaOH, and extracted with dichloromethane. Chromatography was carried out on the oil thus obtained on silica gel using 5% methanol/methylene chloride. The product thus obtained (30 mg, 0.5 mmol) was dissolved in 5 ml of ethanol, and treated with 10% Pd/C (wetted with butanol) (10 mg). The flask was flushed with H2, and stirred under an atmosphere of H2 for 18 hours. After this time, TLC showed some starting material, so an additional 7 mg of 10% Pd/C was added, and the reaction mixture placed again under H2. After 24 additional hours, the solvents were removed using a roto-evaporator, and the residue treated with 1% acetic acid in water. The solution was filtered, and purified using HPLC. This afforded 19 mg of the desired product as a white powder. Overall yield: 10%. NMR (CD3OD): 7.79 ("t", 1H, J=8.1); 7.22 (m, 5H); 6.81 (d, 1H, J=9.0); 6.73 (d, 1H, J=7.2); 4.74 ("t", 1H, J=5.1); 4.61 (m, 1H); 3.85 (s, 2H); 3.18 ("a-b"d, 1H, J=4.5); 3.02 (m, 3H); 2.79 ("a-b"d, 1H, J=5.0); 2.66 (m, 3H). Mass spectrum: 484 (m-H)- ; 598 (M+CF3COO-). EA: Calculated for C23H27N5O7.2.5 F3C3O2H.2.5 H2O: C, 41.24; H, 4.22; N, 8.59. Found: C, 41.30; H, 4.26; N, 8.81.

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