4-Methylmorpholine → 2-(2-nitro-1H-imidazol-1-yl)-N-(2-fluoro-allyl)acetamide

HRID 1766624ノート

反応式

HRID 1766624 の反応式
CN1CCOCC1.[N+:8]([C:11]1[N:12]([CH2:16][C:17]([OH:19])=O)[CH:13]=[CH:14][N:15]=1)([O-:10])=[O:9].ClC(OCC(C)C)=O.Cl.[F:29][C:30](=[CH2:33])[CH2:31][NH2:32]>C1COCC1>[N+:8]([C:11]1[N:12]([CH2:16][C:17]([NH:32][CH2:31][C:30]([F:29])=[CH2:33])=[O:19])[CH:13]=[CH:14][N:15]=1)([O-:10])=[O:9]

参加物

6

反応物 4

HCID 79724-Methylmorpholine2 回HCID 62365Isobutyl chloroformateHCID 3275442-(2-Nitroimidazol-1-yl)acetic acidHCID 167237042-Fluoroprop-2-en-1-amine hydrochloride

生成物 1

HCID 211116852-(2-nitro-1H-imidazol-1-yl)-N-(2-fluoro-allyl)acetamide収率 50%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

N-methylmorpholine (1.01 g, 10 mmol) was added to 2-(2-nitro-1H-imidazol-1-yl)-acetic acid (1.71 g, 10 mmol) in 150 mL of dry THF under nitrogen at 0° C. and stirred for 10 minutes. Isobutyl chloroformate (1.43 mL, 11 mmol) was added. After 30 minutes, 2-fluoro allyl amine hydrochloride (1.23 g, 11 mmol) and N-methylmorpholine (1.21 g, 12 mmol) was added to the solution and the mixture was stirred at room temperature overnight. The solution was filtered and the organic solvent evaporated to give a yellow solid. Purified by column afforded a light yellow solid (1.1 g, 50%).

後処理

  1. waitAfter 30 minutes
  2. stirringthe mixture was stirred at room temperature overnight
  3. filtrationThe solution was filtered
  4. customthe organic solvent evaporated
  5. customto give a yellow solid
  6. customPurified by column

出典と根拠

ORDレコード
ord-a82114286f294498a98d8d838d8fa791
出典データセット
uspto-grants-2007_06
特許番号
US07230115B1

反応ノート

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