反応 #531775

ord-f36af1f0c6ba4cc79e10cd5b4f7447ae

反応方程式

C1CCC(NC2CCCCC2)CC1
dicyclohexylamine
C[C@@H](NC(=O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)OC(C)(C)C)C(=O)NCC(=O)O
Nα -t-butyloxycarbonyl-O-benzyl-L-tyrosyl-D-alanyl-glycine
C(=NC1CCCCC1)=NC1CCCCC1
DCC
COC(=O)[C@@H](N)Cc1ccccc1
L-phenylalanine, methyl ester
COC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](C)NC(=O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)OC(C)(C)C
title compound
収率 82.0%
COC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](C)NC(=O)[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)OC(C)(C)C
Nα -t-Butyloxycarbonyl-O-benzyl-L-tyrosyl-D-alanyl-glycyl-L-phenylalanine, methyl ester
収率 82.0%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe mixture was stirred for 5 minutes at 0° C.
  2. 2
    workup.STIRRINGStirring
  3. 3
    workup.WAITat room temperature for 48 hours
  4. 4
    温度The reaction mixture was cooled to 0° C.
  5. 5
    その他the resulting precipitate was collected
  6. 6
    濃縮The filtrate was concentrated in vacuo
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
  8. 8
    抽出the ethyl acetate solution was extracted successively with 1 N sodium bicarbonate, water, 0.75 N citric acid, and water
  9. 9
    乾燥The ethyl acetate solution was dried over magnesium sulfate
  10. 10
    濃縮concentrated in vacuo
  11. 11
    その他The resulting oil was crystallized from ether
  12. 12
    その他recrystallized from ethyl acetate

実験手順

To 30 ml. of DMF were added 2.5 gms. (0.005 moles) of Nα -t-butyloxycarbonyl-O-benzyl-L-tyrosyl-D-alanyl-glycine (prepared as in Example 1) and 1.08 gms. (0.005 moles) of the hydrochloride salt of L-phenylalanine, methyl ester. The mixture was stirred at 0° C., and 0.99 ml. (0.005 moles) of dicyclohexylamine was added. The mixture was stirred for 5 minutes at 0° C., and 670 mg. (0.005 mmoles) of HBT and 1.03 gms. (0.005 moles) of DCC were added. Stirring was continued at 0° C. for 2 hours and then at room temperature for 48 hours. The reaction mixture was cooled to 0° C., and the resulting precipitate was collected. The filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate, and the ethyl acetate solution was extracted successively with 1 N sodium bicarbonate, water, 0.75 N citric acid, and water. The ethyl acetate solution was dried over magnesium sulfate and concentrated in vacuo. The resulting oil was crystallized from ether and recrystallized from ethyl acetate to give 2.7 grams (82%) of the title compound, m.p. 149°-152° C. [α]D25 +22° (C=0.5, MeOH).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04264491uspto-grants-1981_04