تفاعل #1702121

ord-952d50559a354710a40d35e34981f659

معادلة التفاعل

O=C([O-])O.[Na+]
NaHCO3
BrB(Br)Br
boron tribromide
COc1cccc(CNc2nc(Nc3cccc(CCCO)c3)ncc2Cl)c1
3-[3-({5-chloro-4-[(3-methoxybenzyl)amino]pyrimidin-2-yl}amino)phenyl]propan-1-ol
Oc1cccc(CNc2nc(Nc3cccc(CCCBr)c3)ncc2Cl)c1
desired product
المردود 74.0%
Oc1cccc(CNc2nc(Nc3cccc(CCCBr)c3)ncc2Cl)c1
3-{[(2-{[3-(3-Bromopropyl)phenyl]amino}-5-chloropyrimidin-4-yl)amino]methyl}phenol
المردود 74.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    درجة الحرارةto warm up to rt
  3. 3
    استخلاصThe aqueous layer was extracted with DCM twice
  4. 4
    أخرىdried
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated under vacuum

الإجراء التجريبي

Into a 1-neck round-bottom flask were added 3-[3-({5-chloro-4-[(3-methoxybenzyl)amino]pyrimidin-2-yl}amino)phenyl]propan-1-ol (0.18 g, 0.45 mmol) and DCM (5 mL). To the reaction mixture was added a solution of boron tribromide in methylene chloride (3.0 mL, 3.0 mmol, 1.0 M) at 0° C. The mixture was allowed to warm up to rt and stirred overnight. The resultant mixture was cooled in a dry ice bath when NaHCO3 (saturated aqueous solution, 10 mL) was added. The mixture was allowed to warm up to rt and DCM was added. The aqueous layer was extracted with DCM twice. The organic layers were combined, dried, filtered, and concentrated under vacuum to give the desired product as an off-white powder (150 mg, 74%). LCMS for C20H21BrClN4O (M+H)+: m/z=447.0, 449.0.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08765727B2uspto-grants-2014_07