반응 #6575

ord-50dfb916fc1b4933aac44bd6fca31f18

반응 방정식

COC(=O)[C@@H](N)Cc1ccccc1
phenylalanine methyl ester
O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
trifluoromethanesulfonic anhydride
CCCCc1ncc(CCO)n1Cc1ccccc1Cl
2-n-butyl-1-(2-chlorophenyl)methyl-5-(2-hydroxyethyl)-1H-imidazole
CCN(C(C)C)C(C)C
diisopropylethylamine
CCCCc1ncc(CCN[C@@H](Cc2ccccc2)C(=O)OC)n1Cc1ccccc1Cl
N-[2-{1-[(2 chlorophenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}ethyl ]phenylalanine methyl ester
수율 65.0%

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThis mixture was stirred for 2 hours at -78° C. and an additional 18 hours at ambient temperature
  2. 2
    세척The reaction mixture was washed with water
  3. 3
    기타dried
  4. 4
    농축concentrated
  5. 5
    기타chromatographed with 5% methanol in ethyl acetate

실험 절차

A solution of trifluoromethanesulfonic anhydride (0.954 g, 3.38 mmol) in methylene chloride (5 ml) was cooled to -78° C. under nitrogen, and a solution of 2-n-butyl-1-(2-chlorophenyl)methyl-5-(2-hydroxyethyl)-1H-imidazole (0.9 g, 3.07 mmol), diisopropylethylamine (0.44 g. 3.38 mmol) and methylene chloride (10 ml) was added dropwise. The mixture was stirred at -78° C. for an additional 15 minutes, then a solution of the free base of phenylalanine methyl ester (prepared from 1.33 q (6.15 mmol) of the hydrochloride salt) in methylene chloride (10 ml) was added. This mixture was stirred for 2 hours at -78° C. and an additional 18 hours at ambient temperature. The reaction mixture was washed with water, dried and concentrated and the crude product was flash chromatographed with 5% methanol in ethyl acetate to yield 0.9 g (65%) of N-[2-{1-[(2 chlorophenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}ethyl ]phenylalanine methyl ester.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05248689uspto-grants-1993_09