تفاعل #89835

ord-4d9bfd94fae54af5a79255f6e080a2cb

معادلة التفاعل

[Cl-]
chloride
CCN(CC)CC
Et3N
CC(C)(C)OC(=O)n1ncc2cc(Nc3nc(-c4cccc(N)c4)nc4ccccc34)ccc21
tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
O=C(Cl)N1CCOCC1
morpholine-4-carbonyl chloride
O=C(Cl)N1CCOCC1
morpholine-4-carbonyl chloride
CCN(CC)CC
Et3N
CCN(CC)CC
Et3N
CC(C)(C)OC(=O)n1ncc2cc(Nc3nc(-c4cccc(NC(=O)N5CCOCC5)c4)nc4ccccc34)ccc21
tert-butyl 5-(2-(3-(morpholine-4-carboxamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    workup.ADDITIONwere added
  3. 3
    تركيزThe reaction was concentrated in vacuo
  4. 4
    أخرىthe residue was purified by flash chromatography on silica (12:1 CH2Cl2:MeOH)

الإجراء التجريبي

To a suspension of tert-butyl 5-(2-(3-aminophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (100 mg, 0.22 mmol) and morpholine-4-carbonyl chloride (51 μL, 0.44 mmol,) in CH2Cl2 (2 mL) was added Et3N (61 μL, 0.44 mmol) and catalytic amount of DMAP. The reaction mixture was stirred at RT for 2 h after which 2 equivalents each of morpholine-4-carbonyl chloride and Et3N were added. After 2 h of stirring another 2 equivalents of both the chloride and Et3N were added and continued to stir at ambient temperature for 16 hours. The reaction was concentrated in vacuo and the residue was purified by flash chromatography on silica (12:1 CH2Cl2:MeOH). The product tert-butyl 5-(2-(3-(morpholine-4-carboxamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate was isolated. (80 mg, 65%)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440961B2uspto-grants-2016_09