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Hydrochloric Acid → HCID 66727899、化合物

HRID 573267
ノート
印刷プレビュー

反応式

HRID 573267 の反応式
[CH3:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=2)=[CH:3]1.[Cl:18][C:19]1[O:20][C:21]2[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=2[N:23]=1.Cl.O1CCOCC1>CN1CCCC1=O.CCOC(C)=O>[ClH:18].[CH3:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[C:4]([C:11]2[CH:17]=[CH:16][C:14]([NH:15][C:19]3[O:20][C:21]4[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=4[N:23]=3)=[CH:13][CH:12]=2)=[CH:3]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

7

反応物 4

HCID 313Hydrochloric AcidHCID 119862-ChlorobenzoxazoleHCID 312751,4-DioxaneHCID 86688956HCID 86688956、化合物

生成物 1

HCID 66727899HCID 66727899、化合物収率 50.8%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒
HCID 13387
N-methyl-2-pyrrolidone
溶媒

反応条件

温度
120 °C

実験手順

A mixture of 4-(1-methyl-1H-pyrrolo[3,2-b]pyridin-3-yl)aniline (70 mg) and 2-chlorobenzo[d]oxazole (57 mg) in 1-methylpyrrolidinone (2 mL) was stirred at 120° C. for 30 min. After this time, the reaction was cooled to room temperature, diluted with AcOEt (50 mL), washed with saturated NaHCO3 aqueous solution (50 mL), water (2×50 mL) then brine (50 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (CH2Cl2 to 1:19 MeOH/CH2Cl2), dissolved in 1,4-dioxane (2 ml), treated with 4 M HCl in 1,4-dioxane (0.500 mL, 2.00 mmol) and concentrated under reduced pressure. The residue obtained was triturated with boiling is CH3CN to give the title compound (60 mg).

後処理

  1. temperatureAfter this time, the reaction was cooled to room temperature
  2. washwashed with saturated NaHCO3 aqueous solution (50 mL), water (2×50 mL)
  3. dry with materialbrine (50 mL), dried over Na2SO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe residue obtained
  7. customwas purified by silica gel column chromatography (CH2Cl2 to 1:19 MeOH/CH2Cl2)
  8. dissolutiondissolved in 1,4-dioxane (2 ml)
  9. concentrationconcentrated under reduced pressure
  10. customThe residue obtained
  11. customwas triturated with boiling

出典と根拠

ORDレコード
ord-edfc902896d844938e2eeed2fb5adfad
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09029536B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート