반응 #1537895

ord-11d7b575dc2a42e694559ae489af15f3

반응 방정식

CC(C)(C)OC(=O)NCCC1CCNC1
(3RS)-3-(N-tertbutyloxycarbonylaminoethyl) 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
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
(3RS) -1-(N-benzyloxycarbonylamidino)-3-aminoethyl pyrrolidine

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 CH2Cl2
  6. 6
    건조The combined organic layer was dried (Na2SO4)
  7. 7
    여과filtered
  8. 8
    기타evaporated

실험 절차

2.18 g (0.0102 mmole) (3RS)-3-(N-tertbutyloxycarbonylaminoethyl) 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 CH2Cl2. 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: US05602253uspto-grants-1997_02