Cesium carbonate → Methyl 1-cyclopentyl-6-oxo-5-(pyrrolidin-1-yl)-1,6-dihydropyridine-3-carboxylate

HRID 253094ノート

反応式

HRID 253094 の反応式
Br[C:2]1[C:7](=[O:8])[N:6]([CH:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)[CH:5]=[C:4]([C:14]([O:16][CH3:17])=[O:15])[CH:3]=1.[NH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1.C(=O)([O-])[O-].[Cs+].[Cs+]>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH:9]1([N:6]2[C:7](=[O:8])[C:2]([N:18]3[CH2:22][CH2:21][CH2:20][CH2:19]3)=[CH:3][C:4]([C:14]([O:16][CH3:17])=[O:15])=[CH:5]2)[CH2:13][CH2:12][CH2:11][CH2:10]1

参加物

5

反応物 3

HCID 10796Cesium carbonateHCID 31268PyrrolidineHCID 15946267Methyl 5-bromo-1-cyclopentyl-6-oxo-1,6-dihydropyridine-3-carboxylate

生成物 1

HCID 66845136Methyl 1-cyclopentyl-6-oxo-5-(pyrrolidin-1-yl)-1,6-dihydropyridine-3-carboxylate

試薬・触媒・溶媒 1

HCID 9811564Bis(dibenzylideneacetone)palladium触媒

反応条件

温度
95 °C

実験手順

A mixture of methyl 5-bromo-1-cyclopentyl-6-oxo-1,6-dihydropyridine-3-carboxylate (100 mg, 0.33 mmol), pyrrolidine (33 uL, 0.40 mmol), cesium carbonate (150 mg, 0.46 mmol), tris(dibenzylideneacetone)dipalladium (0) (3 mg, 0.0033 mmol), rac-2-2′-bis(diphenyl-phosphino)-1,1′-binaphthyl (3.1 mg, 0.005 mmol) was purged with nitrogen for 30 min, followed by the addition of anhydrous toluene (1.5 mL). The resulting light-brown solution was heated to 95° C. for 17. The mixture was brought to room temperature and partitioned between ethyl acetate and saturated NH4Cl. The organic phase was separated, washed with saturated NH4Cl, brine, dried over MgSO4 and chromatographed on silica gel using 3:1 hexanes:ethyl acetate to afford the title compound as a yellow oil. MS m/z: 291(M+1).

後処理

  1. customwas purged with nitrogen for 30 min
  2. additionfollowed by the addition of anhydrous toluene (1.5 mL)
  3. customwas brought to room temperature
  4. custompartitioned between ethyl acetate and saturated NH4Cl
  5. customThe organic phase was separated
  6. washwashed with saturated NH4Cl, brine
  7. dry with materialdried over MgSO4
  8. customchromatographed on silica gel using 3:1 hexanes

出典と根拠

ORDレコード
ord-b22dc5731509481dacf9843455718a7c
出典データセット
uspto-grants-2011_01
特許番号
US07872009B2

反応ノート

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