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Water → 5-(2-Fluorophenyl)-N-methyl-1H-pyrrole-3-methanamine

HRID 1051001
ノート
印刷プレビュー

反応式

HRID 1051001 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:12][CH:11]=[C:10]([CH:13]=O)[CH:9]=1.[BH4-].[Na+].O.[CH3:18][NH2:19]>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:12][CH:11]=[C:10]([CH2:13][NH:19][CH3:18])[CH:9]=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 4

HCID 962WaterHCID 6329MethylamineHCID 4311764Sodium borohydrideHCID 469085935-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde

生成物 1

HCID 901686945-(2-Fluorophenyl)-N-methyl-1H-pyrrole-3-methanamine

実験手順

5-(2-Fluorophenyl)-1H-pyrrol-3-carboxaldehyde 1d (1.89 g, 10 mmol, prepared by a known method disclosed in “Journal of Medicinal Chemistry”, 2012, 55(9), 4446-4456) was dissolved in 20 mL of methylamine, and the reaction solution was stirred for 1 h. Sodium borohydride (1.14 g, 30 mmol) was added and continuously stirred for 1 h. 10 mL of water were added to the reaction solution, and the reaction solution was concentrated under reduced pressure to obtain the title product 1-(5-(2-fluorophenyl)-1H-pyrrol-3-yl)-N-methylmethanamine 1e (2.0 g, a yellow oil), which was used directly in the next step.

後処理

  1. stirringcontinuously stirred for 1 h
  2. concentrationthe reaction solution was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-2e8aa4c858c547eb8a8acded736bda9d
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09388133B2

反応ノート

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