반응 #3710

ord-f6499446098b4662863c12a5e1de6a7c

반응 방정식

CCOC(C)=O.ClCCl
ethyl acetate methylene chloride
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine
CCN(CC)CC
triethylamine
CC(C)COC(=O)Cl
isobutylchloroformate
CCCCOC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
10,11-Dihydro-10-[4-[(3-methylpropyloxycarbonyl)amino]benzoyl]-5H-pyrrolo[2,1-c][1,4]benzodiazepine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타quenched with 1N NaOH
  2. 2
    기타The organic layer is evaporated in vacuo to a residue which
  3. 3
    workup.STIRRINGis stirred in 5 ml of tetrahydrofuran for 1 hour
  4. 4
    기타evaporated in vacuo to a residue
  5. 5
    추출The residue is extracted with ethyl acetate-methylene chloride
  6. 6
    세척washed with brine
  7. 7
    건조dried (Na2SO4)
  8. 8
    여과filtered through hydrous magnesium silicate
  9. 9
    기타evaporated in vacuo
  10. 10
    기타to give a residue which
  11. 11
    기타to give 0.22 g of cream

실험 절차

To a stirred solution of 0.15 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 2 ml of methylene chloride is added 0.10 g of triethylamine followed by 0.10 g of isobutylchloroformate. The reaction mixture is stirred for 3 hours and then quenched with 1N NaOH. The organic layer is evaporated in vacuo to a residue which is stirred in 5 ml of tetrahydrofuran for 1 hour, then evaporated in vacuo to a residue. The residue is extracted with ethyl acetate-methylene chloride, washed with brine, dried (Na2SO4), filtered through hydrous magnesium silicate and evaporated in vacuo to give a residue which is stirred with ethyl acetate-methylene chloride to give 0.22 g of cream colored solid. MS(CI): 404 (M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733905uspto-grants-1998_03