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Water → Ethyl 8-Fluoro-6-iodo-1-(methylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylate

HRID 1168534
ノート
印刷プレビュー

反応式

HRID 1168534 の反応式
FC(F)(F)C(O)=O.C(O[C:13]([N:15](C)[N:16]1[C:25]2[C:20](=[CH:21][C:22]([I:27])=[CH:23][C:24]=2[F:26])[C:19](=[O:28])[C:18]([C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:17]1)=O)(C)(C)C.C(=O)(O)[O-].[Na+].O>C(Cl)Cl>[F:26][C:24]1[CH:23]=[C:22]([I:27])[CH:21]=[C:20]2[C:25]=1[N:16]([NH:15][CH3:13])[CH:17]=[C:18]([C:29]([O:31][CH2:32][CH3:33])=[O:30])[C:19]2=[O:28]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6422Trifluoroacetic acidHCID 516892Sodium BicarbonateHCID 12083058Ethyl 1-((tert-Butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate

生成物 1

HCID 12083059Ethyl 8-Fluoro-6-iodo-1-(methylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylate収率 98%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒
2 回

実験手順

A solution of trifluroacetic acid (6.40 g) in methylene chloride (5 mL) is added dropwise over a 4 minute period to a solution of ethyl 1-((tert-butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate (Preparation 34, 1.10 g) in methylene chloride (20 mL) at room temperature. After 3.5 h, the mixture is poured into a mixture of saturated sodium bicarbonate solution (125 mL) and water (50 mL), and extracted two times with ethyl acetate. The combined organic extracts are dried (Na2SO4) and concentrated at reduced pressure. The resulting gummy solid is stirred with diethyl ether at room temperature to afford 0.857 g (98%) of the title compound as a white solid.

後処理

  1. extractionextracted two times with ethyl acetate
  2. dry with materialThe combined organic extracts are dried (Na2SO4)
  3. concentrationconcentrated at reduced pressure

出典と根拠

ORDレコード
ord-6962e63c3a1646fda836dbffdede0ffd
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06624159B2

反応ノート

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