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Ammonium Hydroxide → 4-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide

HRID 2091683
ノート
印刷プレビュー

反応式

HRID 2091683 の反応式
[C:1]([C:3]1[C:4]([I:13])=[C:5]([C:10](O)=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2].Cl.C[N:16](C)CCCN=C=NCC.ON1C2C=CC=CC=2N=N1.[OH-].[NH4+]>C(Cl)Cl.CO.O>[C:1]([C:3]1[C:4]([I:13])=[C:5]([C:10]([NH2:16])=[O:11])[S:6][C:7]=1[S:8][CH3:9])#[N:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 14923Ammonium HydroxideHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 580228624-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid

生成物 1

HCID 580228964-Cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxamide

試薬・触媒・溶媒 3

HCID 887
Methanol
溶媒
HCID 962Water溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

To a suspension of 4-cyano-3-iodo-5-(methylsulfanyl)thiophene-2-carboxylic acid (2.85 g, 7.93 mmol) in methylene chloride (30 mL), were added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (3.28 g, 17.1 mmol) and 1-hydroxybenzotriazole (2.27 g, 16.8 mmol). The reaction mixture was stirred at room temperature for two hours and ammonium hydroxide (15.4 mL) was added and the biphasic mixture was stirred at room temperature for two hours. Water (100 mL), methanol (50 mL), methylene chloride (200 mL) was added. The organic layer was removed. The aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to the title compound as dark red oil (1.47 g, 57%). LCMS: (FA) ES+ 325.

後処理

  1. stirringthe biphasic mixture was stirred at room temperature for two hours
  2. customThe organic layer was removed
  3. extractionThe aqueous layer was extracted five times with a solution of 20% methanol in methylene chloride (100 mL)
  4. dry with materialThe combined organic extracts were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated to the title compound as dark red oil (1.47 g, 57%)

出典と根拠

ORDレコード
ord-a2a59f775e0843cf96eb6befe588ba8a
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08440664B2

反応ノート

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