Ammonium Chloride → N-(5-{[2-({[2-(hydroxymethyl)cyclopropyl]carbonyl}amino)imidazo[1,2-b]pyridazin-6-yl]oxy}-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide

HRID 2391425

反応式

HRID 2391425 の反応式
[Cl-].[Ca+2].[Cl-].[BH4-].[Na+].[CH3:6][N:7]1[C:11]([C:12]([NH:14][C:15]2[CH:16]=[C:17]([CH:38]=[CH:39][C:40]=2[CH3:41])[O:18][C:19]2[CH:20]=[CH:21][C:22]3[N:23]([CH:25]=[C:26]([NH:28][C:29]([CH:31]4[CH2:33][CH:32]4[C:34](OC)=[O:35])=[O:30])[N:27]=3)[N:24]=2)=[O:13])=[CH:10][C:9]([CH3:42])=[N:8]1.[Cl-].[NH4+]>O1CCCC1.C(O)C.C(OCC)(=O)C>[OH:35][CH2:34][CH:32]1[CH2:33][CH:31]1[C:29]([NH:28][C:26]1[N:27]=[C:22]2[CH:21]=[CH:20][C:19]([O:18][C:17]3[CH:38]=[CH:39][C:40]([CH3:41])=[C:15]([NH:14][C:12]([C:11]4[N:7]([CH3:6])[N:8]=[C:9]([CH3:42])[CH:10]=4)=[O:13])[CH:16]=3)=[N:24][N:23]2[CH:25]=1)=[O:30]

参加物

7

反応物 4

HCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 5284359Calcium ChlorideHCID 57505658HCID 57505658、化合物

生成物 1

HCID 57505665N-(5-{[2-({[2-(hydroxymethyl)cyclopropyl]carbonyl}amino)imidazo[1,2-b]pyridazin-6-yl]oxy}-2-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide収率 20%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒HCID 21873804Tetrahydrofuran ethanol溶媒2 回

実験手順

To a suspension of calcium chloride (135 mg, 1.1 mmol) in tetrahydrofuran/ethanol (2/1, 1 mL) was added a solution of sodium borohydride (92 mg, 2.2 mmol) and methyl 2-({[6-(3-{[(1,3-dimethyl-1H-pyrazol-5-yl)carbonyl]amino}-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]amino}carbonyl)cyclopropanecarboxylate (180 mg, 0.37 mmol) in tetrahydrofuran/ethanol (2/1, 1 mL), and the mixture was stirred at room temperature for 18 hr. Saturated aqueous ammonium chloride solution and ethyl acetate were added to the reaction mixture, and the aqueous layer was extracted with ethyl acetate (×3). Combined organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=40/60→100/0, and then methanol/ethyl acetate=0/100→5/95) to give the title compound (35 mg, 20%) as a white solid.

後処理

  1. extractionthe aqueous layer was extracted with ethyl acetate (×3)
  2. washCombined organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltrated
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane=40/60→100/0

出典と根拠

ORDレコード
ord-0adeb9f7203d4ddca79052d67f2e354c
出典データセット
uspto-grants-2012_09
特許番号
US08273741B2

関連ノート

読み込み中…