반응 #73345

ord-d3489b4f83bf434abc1caf76276e89cf

반응 방정식

NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3cccc(C(F)(F)F)c3)c2)ncn1
5-(6-aminomethyl-pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide
C1CCOC1
THF
CN(C)C(=O)Cl
dimethylcarbamyl chloride
CN(C)C(=O)NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3cccc(C(F)(F)F)c3)c2)ncn1
title compound
CN(C)C(=O)NCc1cc(Oc2ccc3c(ccn3C(=O)Nc3cccc(C(F)(F)F)c3)c2)ncn1
5-[6-(3,3-Dimethyl-ureidomethyl)-pyrimidin-4-yloxy]-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After 10 min the solution is partitioned between EtOAc and water
  2. 2
    기타The organic layer is separated
  3. 3
    세척washed further with brine
  4. 4
    건조dried over Na2SO4
  5. 5
    여과filtered
  6. 6
    농축concentrated under reduced pressure

실험 절차

To a solution of 5-(6-aminomethyl-pyrimidin-4-yloxy)-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide (50 mg, 0.12 mmol), THF (5 mL), and dimethylcarbamyl chloride (50 mg) is added triethylamine (50 mg). After 10 min the solution is partitioned between EtOAc and water. The organic layer is separated and washed further with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541432B2uspto-grants-2013_09