Reaktion #969860

Reaktionsgleichung

4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butanoic acid

tert-butyl 3-(2-(2-(2-aminoacetamido)acetamido)acetamido)propanoate

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

→

title compound

Ausbeute 78.4%

Gaba Gly-Gly-Gly-β-Ala-OtBu

Ausbeute 78.4%

Lösungsmittel

dimethyl formamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction mixture was purified in four equal portions by reverse phase HPLC
2. 2
   WaschenThe column was eluted at 100 mL/min with deionized water containing 0.3% formic acid and 5% acetonitrile for 10 min
3. 3
   workup.WAITfollowed by a 13 min linear gradient from 5% acetonitrile to 33% acetonitrile
4. 4
   Sonstigesolvent was removed by rotary evaporation under vacuum

Vorschrift

513 mg (2.8 mmol) of 4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butanoic acid, 800 mg (0.2.8 mmol) tert-butyl 3-(2-(2-(2-aminoacetamido)acetamido)acetamido)propanoate and 583 mg (3.0 mmol) N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride were disolved in 12 mL of dimethyl formamide and stirred for 3 hours. The reaction mixture was purified in four equal portions by reverse phase HPLC using a 5.0 cm×25 cm C18 column. The column was eluted at 100 mL/min with deionized water containing 0.3% formic acid and 5% acetonitrile for 10 min followed by a 13 min linear gradient from 5% acetonitrile to 33% acetonitrile. Product fractions (retention time of 21 min) were combined and solvent was removed by rotary evaporation under vacuum to give 832 mg (62%) of the title compound. 1H NMR (d6-DMSO) 8.10-8.16 (m, 2H), 8.07 (t, J=4.8 Hz, 1H), 7.0-7.15 (m, 1H), 3.747 (t, J=6.0 Hz, 3H), 3.64 (d, J=5.6 Hz, 2H), 3.41 (t, J=6.8, 2H), 3.1-3.33 (m, 1H), 3.19-3.26 (m, 2H), 2.348 (t, J=6.8, 2H), 2.132 (t, J=7.2 Hz, 2H), 1.67-1.76 (m, 2H), 1.39 (s, 9H). 13C NMR (d6-DMSO) 171.80, 170.98, 170.39, 169.48, 168.96, 168.56, 134.37, 79.83, 42.05, 41.83, 37.38, 34.82, 34.71, 32.26, 27.83, 23.95. HRMS (M+Na+) Calc. 504.2070 found 504.2046

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