تفاعل #959

ord-50d2591cf07947e7ab725904f4df96f4

معادلة التفاعل

CS(=O)(=O)Cl
methanesulphonyl chloride
N=C(NC(=O)OCc1ccccc1)N1CCC(CO)C1
(3RS)-1-(N-benzyloxycarbonylamidino)-3-hydroxymethyl pyrrolidine
CCN(CC)CC
triethylamine
CS(=O)(=O)OCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
title compound
المردود 50.0%
CS(=O)(=O)OCC1CCN(C(=N)NC(=O)OCc2ccccc2)C1
(3RS)-1-(N-benzyloxycarbonylamidino)-3-mesyloxymethyl pyrrolidine
المردود 50.0%

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  3. 3
    استخلاصextracted with a 0.3M KHSO4 -solution
  4. 4
    غسيلThe water layer was washed once with CH2Cl2
  5. 5
    استخلاصextracted twice with CH2Cl2
  6. 6
    أخرىThe combined organic layer was dried (Na2 SO4)
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated

الإجراء التجريبي

0.7 g (2.53 mmole) (3RS)-1-(N-benzyloxycarbonylamidino)-3-hydroxymethyl pyrrolidine and 0.70 ml (5.05 mmole) triethylamine was dissolved in 15 ml diethyl ether/CH2Cl2 1/1 and the mixture was cooled to 0° C. 0.25 ml (3.29 mmole) methanesulphonyl chloride in 3 ml diethyl ether was slowly added and the reaction mixture was stirred at 0° C for three hours. The solvent was evaporated and the residue was dissolved in ethyl acetate and extracted with a 0.3M KHSO4 -solution. The water layer was washed once with CH2Cl2. The water layer was made neutral with 10M NaOH-solution and extracted twice with CH2Cl2. The combined organic layer was dried (Na2 SO4), filtered and evaporated to yield 0.450 g (50%) of the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723444uspto-grants-1998_03