Potassium Phosphate, Tribasic → 2-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamide

HRID 1472573

反応式

HRID 1472573 の反応式
[Cl:1][C:2]1[CH:9]=[C:8](I)[C:5]([C:6]#[N:7])=[CH:4][N:3]=1.[NH2:11][C:12]1[CH:22]=[CH:21][CH:20]=[CH:19][C:13]=1[C:14]([NH:16]OC)=[O:15].[O-]P([O-])([O-])=O.[K+].[K+].[K+].[CH:31]1C=CC(P(C2C(OC3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=CC=3)=CC=CC=2)C2C=CC=CC=2)=CC=1>O1CCOCC1.CC(O)=O.CC(O)=O.[Pd]>[Cl:1][C:2]1[CH:9]=[C:8]([NH:11][C:12]2[CH:22]=[CH:21][CH:20]=[CH:19][C:13]=2[C:14]([NH:16][CH3:31])=[O:15])[C:5]([C:6]#[N:7])=[CH:4][N:3]=1

参加物

7

反応物 4

HCID 62657Potassium Phosphate, TribasicHCID 4285986Bis[2-(diphenylphosphino)phenyl] etherHCID 123927072-Amino-N-methoxybenzamideHCID 575169126-Chloro-4-iodopyridine-3-carbonitrile

生成物 1

HCID 575169132-(2-Chloro-5-cyanopyridin-4-ylamino)-N-methylbenzamide収率 740.3%

試薬・触媒・溶媒 2

HCID 4144353Palladium (II) acetate触媒HCID 312751,4-Dioxane溶媒

反応条件

温度
110 °C

実験手順

A mixture of 6-chloro-4-iodo-nicotinonitrile (14 g, 53.03 mmole, 1 eq), 2-amino-N-methoxy-benzamide (7.96 g, 53.03 mmole, 1 eq) and K3PO4 (28.14 g, 132.57 mmole, 2.5 eq) in 1,4-dioxane (250 mL) was degassed with N2 for 1 h. To this mixture were added Pd(OAC)2 (0.238 g, 1.06 mmole, 0.02 eq) and DPEPhos (2.28 g, 4.24 mmole, 0.08 eq). The resulting reaction mixture was degassed with N2 for another 15 min after which the resulting reaction mixture was stirred at 110° C. overnight. After completion of reaction solid material was collected by filtration, dissolved in water (500 mL), and extracted with ethyl acetate (5×200 mL). Combined organic layers were dried over sodium sulfate, filtered and concentrated under reduced pressure to give crude material. It was purified by column chromatography over silica gel (60-120 mesh) using 0.2% methanolic ammonia (10% ammonia in MeOH) in dichloromethane as the eluant to give the title compound as a pale yellow solid (9 g, 59%). 1H-NMR (400 MHz, DMSO-d6): δ 2.75 (d, 3H, J=4.56 Hz), 7.09 (s, 1H), 7.25-7.35 (m, 1H), 7.53-7.60 (m, 2H), 7.72 (d, 1H, J=7.48 Hz), 8.56 (s, 1H), 8.69-8.79 (brs, 1H), 10.65 (s, 1H). LC-MS calculated for C14H11ClN4O (M+H) 287.06. found 286.9.

後処理

  1. customwas degassed with N2 for 1 h
  2. customThe resulting reaction mixture
  3. customwas degassed with N2 for another 15 min after which
  4. customthe resulting reaction mixture
  5. customAfter completion of reaction solid material
  6. filtrationwas collected by filtration
  7. dissolutiondissolved in water (500 mL)
  8. extractionextracted with ethyl acetate (5×200 mL)
  9. dry with materialCombined organic layers were dried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure
  12. customto give crude material
  13. customIt was purified by column chromatography over silica gel (60-120 mesh)

出典と根拠

ORDレコード
ord-96c5f4f1208a49b7817fe80ec6b61e7a
出典データセット
uspto-grants-2015_04
特許番号
US09012479B2

関連ノート

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