반응 #8704

ord-d9955e3e540d4e58a5a30ceda7476e84

반응 방정식

COc1cccc(Oc2c(Cl)nc(N3CCOCC3)nc2NS(=O)(=O)CCc2ccccc2)c1
2-phenyl-ethanesulfonic acid [6-chloro-5-(3-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl]-amide
OCCO
ethylene glycol
COc1cccc(Oc2c(NS(=O)(=O)CCc3ccccc3)nc(N3CCOCC3)nc2OCCO)c1
2phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(3-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl]-amide

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The solution was cooled to rt
  2. 2
    추출extracted twice with EA (150 ml)
  3. 3
    세척The organic phase was washed with water (50 ml)
  4. 4
    기타evaporated
  5. 5
    기타The crude product was purified by chromatography on silica gel eluting with heptane:EA 1:1 to 1:2

실험 절차

A suspension of 2-phenyl-ethanesulfonic acid [6-chloro-5-(3-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl]-amide (1.27 g) in ethylene glycol (12 ml) was treated with K-tert.-butylate (2.82 g). The resulting solution was stirred at 100° C. for 12 d. The solution was cooled to rt, diluted with 10% aq. citric acid (150 ml) and extracted twice with EA (150 ml). The organic phase was washed with water (50 ml) and evaporated. The crude product was purified by chromatography on silica gel eluting with heptane:EA 1:1 to 1:2 to furnish 2phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(3-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl]-amide (1.1 g) as a white solid. LC-MS: tR=4.66 min, [M+1]+=531.20, [M−1]−=529.14.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091201B2uspto-grants-2006_08