تفاعل #11042

ord-796ff312c8e04ffba5526c15fe31e9ab

معادلة التفاعل

Nc1ccccc1N
o-phenylendiamine
CCOC(=O)CC(NS(=O)(=O)c1cccc(-c2cccc(N)c2)c1)c1ccccc1
ethyl 3-{[(3′-amino[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate
S=C(Cl)Cl
thiophosgene
CCOC(=O)CC(NS(=O)(=O)c1cccc(-c2cccc(NC(=S)Nc3ccccc3N)c2)c1)c1ccccc1
Ethyl 3-{[(3′-{[(2-aminoanilino)carbothioyl]amino}[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was refluxed for 2 h
  2. 2
    أخرىevaporated
  3. 3
    workup.DISSOLUTIONthe residue dissolved in 200 ml toluene
  4. 4
    تركيزconcentrated
  5. 5
    أخرىpurified (flash chromatography: dichloromethane/acetic acid ethyl ester 10+1)
  6. 6
    أخرىto yield 43 g (100%)

الإجراء التجريبي

31.84 g (75 mmol) ethyl 3-{[(3′-amino[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate 10.1.2 were dissolved in 600 ml toluene and 8.62 g thiophosgene were added. The mixture was refluxed for 2 h, evaporated and the residue dissolved in 200 ml toluene. This solution was added dropwise to a solution of o-phenylendiamine (12.2 g 113 mmol) in 500 ml tetrahydrofurane/toluene (1/1) at 40° C. The mixture was stirred for 12 h at room temperature, concentrated and purified (flash chromatography: dichloromethane/acetic acid ethyl ester 10+1) to yield 43 g (100%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094911B2uspto-grants-2006_08