(4-Nitrophenyl)acetic acid → di t-butyl 4-nitrobenzylcarbonyl-L-glutamate

HRID 619412

Reaktionsgleichung

Reaktionsgleichung von HRID 619412
[OH:1][N:2]1C2C=CC=CC=2N=N1.[N+]([C:14]1[CH:19]=[CH:18][C:17]([CH2:20][C:21]([OH:23])=O)=[CH:16][CH:15]=1)([O-])=O.[C:24]([O:28][C:29](=[O:41])[C@H:30]([CH2:32][CH2:33][C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[NH2:31])([CH3:27])([CH3:26])[CH3:25].C1(N=C=NC2CCCCC2)CCCCC1.CN(C)C=[O:60]>>[N+:2]([CH:33]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:32][C@@H:30]([C:29]([O:28][C:24]([CH3:26])([CH3:27])[CH3:25])=[O:41])[NH:31][C:21]([CH2:20][C:17]1[CH:16]=[CH:15][CH:14]=[CH:19][CH:18]=1)=[O:23])([O-:1])=[O:60]

Komponenten

6

Versuchsvorschrift

1-Hydroxybenzotriazole (4.05 g) was added to a solution of 4-nitrophenyl acetic acid (5.4 g) in dimethylformamide (75 ml). L-Glutamic acid di tert-butyl ester (7.77 g) and then dicyclohexylcarbodiimide (6.2 g) were added to the mixture. The mixture was then stirred for 18 hr at ambient temperature. The mixture was filtered and the filtrate washed with saturated sodium bicarbonate solution, water and 0.5 m hydrochloric acid and then dried and evaporated to dryness. The residue was chromatographed on silica gel by eluting with hexane/ethyl acetate (2:1) to give di t-butyl 4-nitrobenzylcarbonyl-L-glutamate as an oil 9.7 g (77%). NMR: 8.2(d)2H; 7.45(d)2H; 6.45(d)1H; 4.45(m)1H; 3.15(s)2H; 2.1(m)4H; 1.4(d)9H; 1.35(s)9H.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. washthe filtrate washed with saturated sodium bicarbonate solution, water and 0.5 m hydrochloric acid
  3. customdried
  4. customevaporated to dryness
  5. customThe residue was chromatographed on silica gel
  6. washby eluting with hexane/ethyl acetate (2:1)

Quellen und Nachweise

ORD-Eintrag
ord-fd6a939a4e6146c6a9f212db56b50549
Quelldatensatz
uspto-grants-1999_09
Patentnummer
US05958971

Verknüpfte Notizen

Wird geladen…