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HCID 47453787、化合物 → HCID 59596398、化合物

HRID 2264606
ノート
印刷プレビュー

反応式

HRID 2264606 の反応式
Cl[C:2]1[CH:7]=[C:6]([O:8][C:9]2[CH:10]=[C:11]3[C:16](=[CH:17][CH:18]=2)[N:15]=[CH:14][CH:13]=[CH:12]3)[N:5]=[C:4]([NH2:19])[N:3]=1>C1COCC1.[Pd]>[NH:15]1[C:16]2[C:11](=[CH:10][C:9]([O:8][C:6]3[CH:7]=[CH:2][N:3]=[C:4]([NH2:19])[N:5]=3)=[CH:18][CH:17]=2)[CH2:12][CH2:13][CH2:14]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 47453787HCID 47453787、化合物

生成物 1

HCID 59596398HCID 59596398、化合物

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 5.4 g (0.02 mol) 4-chloro-6-(quinolin-6-yloxy)-pyrimidin-2-ylamine in 600 mL of THF is hydrogenated during 21 h in the presence of 1.2 g Pd/C (10% Engelhard 4505). Then the catalyst is filtered off and the filtrate concentrated in vacuuo. The residue is partitioned between ethyl acetate and conc. sodium bicarbonate solution and the organic layer washed with brine, dried and evaporated. The crude product is purified by flash-chromatography on silica gel using dichloromethane/methanol 95:5 as eluent. Fractions with pure compound are pooled and evaporated. The crystalline material is triturated with ether, filtered and dried to give the title compound: m.p. 180-182° C.; MS: [M+1]+=243; TLC (dichloromethane/methanol 95:5): Rf=0.4.

後処理

  1. filtrationThen the catalyst is filtered off
  2. concentrationthe filtrate concentrated in vacuuo
  3. customThe residue is partitioned between ethyl acetate and conc. sodium bicarbonate solution
  4. washthe organic layer washed with brine
  5. customdried
  6. customevaporated
  7. customThe crude product is purified by flash-chromatography on silica gel
  8. customevaporated
  9. customThe crystalline material is triturated with ether
  10. filtrationfiltered
  11. customdried

出典と根拠

ORDレコード
ord-256ba812e35746868ea1714b7eca2bcd
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07855215B2

反応ノート

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