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Bromine → HCID 86655362、化合物

HRID 2190389
ノート
印刷プレビュー

反応式

HRID 2190389 の反応式
[S-:1][C:2]#[N:3].[K+].[NH2:5][C:6]1[CH:32]=[CH:31][C:9]([O:10][C:11]2[CH:12]=[C:13]([NH:17][C:18](=[O:30])[C:19]3[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([C:28]#[N:29])([CH3:27])[CH3:26])[CH:20]=3)[CH:14]=[CH:15][CH:16]=2)=[C:8]([F:33])[CH:7]=1.BrBr>C(O)(=O)C>[NH2:3][C:2]1[S:1][C:32]2[CH:31]=[C:9]([O:10][C:11]3[CH:12]=[C:13]([NH:17][C:18](=[O:30])[C:19]4[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([C:28]#[N:29])([CH3:27])[CH3:26])[CH:20]=4)[CH:14]=[CH:15][CH:16]=3)[C:8]([F:33])=[CH:7][C:6]=2[N:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24408BromineHCID 516872Potassium thiocyanateHCID 67313673HCID 67313673、化合物

生成物 1

HCID 86655362HCID 86655362、化合物収率 57%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒3 回

実験手順

Potassium thiocyanate (500 mg, 5.12 mmol) was suspended in acetic acid (10 mL) and the mixture was stirred at room temperature for 10 min. To the obtained solution was added a solution of N-[3-(4-amino-2-fluorophenoxy)phenyl]-3-(1-cyano-1-methylethyl)benzamide (500 mg, 1.28 mmol) in acetic acid (10 mL), and the mixture was further stirred at room temperature for 15 min. To the obtained solution was added dropwise slowly a solution of bromine (0.225 g, 1.41 mmol) in acetic acid (7.0 mL) and, after the completion of the dropwise addition, the mixture was stirred at room temperature for 14 hr. The resulting yellow insoluble material was filtrated, and washed with acetic acid. The filtrate and washing were combined and concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate (300 mL), washed with 5% aqueous sodium hydrogencarbonate solution (200 mL×2), water (200 mL) and saturated brine (200 ml), successively, and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (0.32 g, 57%) as a yellow amorphous substance. The obtained compound was used in the next reaction without a further purification.

後処理

  1. stirringthe mixture was further stirred at room temperature for 15 min
  2. additionafter the completion of the dropwise addition
  3. stirringthe mixture was stirred at room temperature for 14 hr
  4. filtrationThe resulting yellow insoluble material was filtrated
  5. washwashed with acetic acid
  6. washThe filtrate and washing
  7. concentrationconcentrated under reduced pressure
  8. washwashed with 5% aqueous sodium hydrogencarbonate solution (200 mL×2), water (200 mL) and saturated brine (200 ml)
  9. dry with materialsuccessively, and dried over anhydrous sodium sulfate
  10. filtrationThe insoluble material was filtered off
  11. concentrationthe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-4128980b54da48a9b42fb37bffb585ad
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324395B2

反応ノート

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