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Water → 4-Chloro-3-(1-morpholin-4-ylphthalazin-6-yl)benzamide

HRID 2357636
ノート
印刷プレビュー

反応式

HRID 2357636 の反応式
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)=[N:7][N:6]=[CH:5]2.C([O-])(=O)C.[K+].CC1(C)C(C)(C)OB(B2OC(C)(C)C(C)(C)O2)O1.[Cl:41][C:42]1[CH:50]=[CH:49][C:45]([C:46]([NH2:48])=[O:47])=[CH:44][C:43]=1I.C(=O)([O-])[O-].[K+].[K+].O>C(OCC)(=O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C(O)C.O1CCOCC1>[Cl:41][C:42]1[CH:50]=[CH:49][C:45]([C:46]([NH2:48])=[O:47])=[CH:44][C:43]=1[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)=[N:7][N:6]=[CH:5]2
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

12

反応物 6

HCID 962WaterHCID 11430Potassium CarbonateHCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 221155764-Chloro-3-iodobenzamideHCID 251294786-Bromo-1-morpholinophthalazine

生成物 1

HCID 68456728
4-Chloro-3-(1-morpholin-4-ylphthalazin-6-yl)benzamide

試薬・触媒・溶媒 5

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)触媒HCID 178418397HCID 178418397、化合物触媒HCID 702Ethanol溶媒HCID 8857Ethyl Acetate溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
80 °C

実験手順

To 6-Bromo-1-morpholinophthalazine (0.20 g, 680 μmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride (50 mg, 68 μmol), potassium acetate (200 mg, 2040 μmol), and 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (207 mg, 816 μmol) was added 1,4-dioxane (6.80 mL) and the mixture was heated to 80° C. for 2 h. The mixture was added to a sealed tube containing 4-chloro-3-iodobenzamide (230 mg, 816 μmol), tetrakis(triphenylphosphine)palladium (79 mg, 68 μmol), potassium carbonate—1.5 M in water (1.81 μl, 2.72 mmol), and ethanol (6.80 mL) and heated to 110° C. for 2 h. After cooling the reaction mixture was diluted with 75 mL of ethyl acetate, added to a separation funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, concentrated in vacuo, and purified by HPLC to give the title compound.

後処理

  1. additionThe mixture was added to a sealed tube
  2. temperatureheated to 110° C. for 2 h
  3. temperatureAfter cooling the reaction mixture
  4. additionadded to a separation funnel
  5. custompartitioned with sodium bicarbonate (saturated, aqueous)
  6. washwashed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous)
  7. customseparated
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated in vacuo
  10. custompurified by HPLC

出典と根拠

ORDレコード
ord-ac43cb98b6b340debbd465fa1b976610
出典データセット
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07759337B2

反応ノート

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