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

HRID 651200

反応式

HRID 651200 の反応式
[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]

参加物

6

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-31560eb9abaa42709ee86dbe8a210f7f
出典データセット
uspto-grants-2001_08
特許番号
US06277880B1

関連ノート

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