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O,O-Dipyridin-2-yl carbonothioate → 6-Isothiocyanato-7-methylindole

HRID 1275657
ノート
印刷プレビュー

反応式

HRID 1275657 の反応式
[NH2:1][C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.C1C=C(O[C:19](OC2N=CC=CC=2)=[S:20])N=CC=1>C(Cl)Cl>[N:1]([C:2]1[C:10]([CH3:11])=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1)=[C:19]=[S:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 719784O,O-Dipyridin-2-yl carbonothioateHCID 158963787-methyl-1H-indol-6-amine

生成物 1

HCID 158963796-Isothiocyanato-7-methylindole収率 70%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a solution of 6-amino-7-methylindole (1.0 g, 6.84 mmol) in methylene chloride (50 mL) is added di-2-pyridyl thionocarbonate (1.59 g, 6.84 mmol). The resulting solution is stirred at room temperature for two hours followed by removal of the methylene chloride by rotary evaporation. The crude material is purified via silica gel column chromatography using 10% ethyl acetate/hexane as the eluting solvent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.90 g of 6-isothiocyanato-7-methylindole as a white solid (70% yield).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customfollowed by removal of the methylene chloride by rotary evaporation
  2. customThe crude material is purified via silica gel column chromatography
  3. additionThe product containing fractions
  4. customthe solvents removed by rotary evaporation

出典と根拠

ORDレコード
ord-d60a1724c27447bea73ce600b591400c
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06162818

反応ノート

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