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Cesium carbonate → 5-Chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-oxo-morpholin-3-yl)-pyridin-2-yl]-amide

HRID 538309
ノート
印刷プレビュー

反応式

HRID 538309 の反応式
C1(P(C2C=CC=CC=2)C2C3OC4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C(C)(C)C=3C=CC=2)C=CC=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[C:50]1[N:55]=[C:54]([C:56]2([CH2:63][F:64])[NH:61][C:60](=[O:62])[CH2:59][O:58][CH2:57]2)[CH:53]=[CH:52][CH:51]=1.[Cl:65][C:66]1[CH:67]=[CH:68][C:69]([C:72]([NH2:74])=[O:73])=[N:70][CH:71]=1>O1CCOCC1.[Pd].[Pd].C(=CC(C=CC1C=CC=CC=1)=O)C1C=CC=CC=1.C(=CC(C=CC1C=CC=CC=1)=O)C1C=CC=CC=1.C(=CC(C=CC1C=CC=CC=1)=O)C1C=CC=CC=1.O>[F:64][CH2:63][C:56]1([C:54]2[N:55]=[C:50]([NH:74][C:72]([C:69]3[CH:68]=[CH:67][C:66]([Cl:65])=[CH:71][N:70]=3)=[O:73])[CH:51]=[CH:52][CH:53]=2)[CH2:57][O:58][CH2:59][C:60](=[O:62])[NH:61]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10796Cesium carbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 218831585-Chloropyridine-2-carboxamideHCID 866680235-(6-Bromo-pyridin-2-yl)-5-fluoromethyl-morpholin-3-one

生成物 1

HCID 866680245-Chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-oxo-morpholin-3-yl)-pyridin-2-yl]-amide

試薬・触媒・溶媒

3
HCID 9832798Tris(dibenzylideneacetone) dipalladium触媒HCID 962Water溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
80 °C

実験手順

A mixture of 4,5-Bis(diphenyl phosphino)-9,9-dimethyl xanthene (0.04 g, 0.069 mmol), tris(dibenzylidene-acetone) di palladium(0) (0.032 g, 0.035 mmol) and cesium carbonate (0.678 g, 2.083 mmol) were taken in 1,4-dioxane and degassed with argon for 10 min. 5-(6-Bromo-pyridin-2-yl)-5-fluoromethyl-morpholin-3-one (0.2 g, 0.694 mmol) followed by 5-chloropicolinamide (0.119 g, 0.764 mmol) were added to the resultant reaction mixture and degassed with argon for further 5 min. Reaction mixture was then heated at 80° C. for 16 h and cooled to rt. Reaction contents were treated with water and product was extracted with ethyl acetate, washed with brine and dried over anhy. Na2SO4. The organic layer was concentrated under reduced pressure to obtain liquid which was triturated with n-pentane to furnish title compound as a off-white solid. Yield=0.24 g (crude). TLC (50% ethyl acetate in hexane) Rf=0.45; LCMS: RtH8=1.215, [M+1]=365.1 and 366.9; HPLC RtH9=4.367 min (53%).

後処理

  1. customdegassed with argon for 10 min
  2. additionwere added to the resultant
  3. customreaction mixture
  4. customdegassed with argon for further 5 min
  5. customReaction mixture
  6. temperaturecooled to rt
  7. customReaction contents
  8. extractionwas extracted with ethyl acetate
  9. washwashed with brine
  10. customdried over anhy
  11. concentrationThe organic layer was concentrated under reduced pressure
  12. customto obtain liquid which
  13. customwas triturated with n-pentane

出典と根拠

ORDレコード
ord-444cdd52e76546678cea8838f56baba8
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08865712B2

反応ノート

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