반응 #1702126

ord-0f64242667f744029fd4af9aa5c881a1

반응 방정식

O=C([O-])O.[Na+]
NaHCO3
BrB(Br)Br
boron tribromide
COc1cccc(CNc2nc(Nc3cccc(OC)c3)ncc2Cl)c1
5-chloro-N(4)-(3-methoxybenzyl)-N(2)-(3-methoxyphenyl)pyrimidine-2,4-diamine
Oc1cccc(CNc2nc(Nc3cccc(O)c3)ncc2Cl)c1
desired product
수율 58.3%
Oc1cccc(CNc2nc(Nc3cccc(O)c3)ncc2Cl)c1
3-({5-Chloro-4-[(3-hydroxybenzyl)amino]pyrimidin-2-yl}amino)phenol
수율 58.3%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    온도to warm up to rt
  3. 3
    추출The aqueous layer was extracted with DCM twice
  4. 4
    기타dried
  5. 5
    여과filtered
  6. 6
    농축concentrated under vacuum

실험 절차

Into a 1-neck round-bottom flask were added 5-chloro-N(4)-(3-methoxybenzyl)-N(2)-(3-methoxyphenyl)pyrimidine-2,4-diamine (90 mg, 0.2 mmol) and methylene chloride (5 mL). To the 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 (40 mg, 50%). LCMS for C17H16ClN4O2 (M+H)+: m/z=343.0.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08765727B2uspto-grants-2014_07