반응 #965

ord-d42f48a7d3fc473aba6c5139093935b5

반응 방정식

CC(C)(C)OC(=O)NCCC1CCNC1
(3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine
CSC(=N)NC(=O)OCc1ccccc1
N-benzyloxycarbonyl-S-methylisothiourea
O=S(=O)([O-])O.[K+]
KHSO4
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
title compound
수율 67.5%
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
(3RS)-1-(N-benzyloxycarbonylamidino)-3-aminoethyl pyrrolidine
수율 67.5%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도heated to 60°-70° C. for eight hours
  2. 2
    세척the water layer was washed with a mixture of the toluene and ethyl acetate
  3. 3
    workup.WAITleft for 2 days under which time the Boc group
  4. 4
    기타was removed
  5. 5
    추출extracted four times with CH2 Cl2
  6. 6
    건조The combined organic layer was dried (Na2SO4)
  7. 7
    여과filtered
  8. 8
    기타evaporated

실험 절차

2.18 g (0.0102 mole) (3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine and 2.81 g (0.0125 mole) N-benzyloxycarbonyl-S-methylisothiourea was dissolved in 30 ml toluene and heated to 60°-70° C. for eight hours followed by stirring at room temperature for one day. 0.3M KHSO4 -solution was added and the water layer was washed with a mixture of the toluene and ethyl acetate and left for 2 days under which time the Boc group was removed. The acidic water phase was made alkaline and extracted four times with CH2 Cl2. The combined organic layer was dried (Na2SO4), filtered and evaporated to yield 2.0 g (51%) of the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723444uspto-grants-1998_03