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Ethoxalyl chloride → 1-(2,4-Difluoro-phenyl)-3-(2,2-dimethyl-propyl)-2-thioxo-imidazolidine-4,5-dione

HRID 1241624
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HRID 1241624 반응식
Cl[C:2](=[O:8])[C:3]([O:5]CC)=O.[F:9][C:10]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=1[NH:17][C:18]([NH:20][CH2:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[S:19]>ClCCl>[F:9][C:10]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=1[N:17]1[C:2](=[O:8])[C:3](=[O:5])[N:20]([CH2:21][C:22]([CH3:24])([CH3:23])[CH3:25])[C:18]1=[S:19]
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참가 물질

4

반응물 2

HCID 20884Ethoxalyl chlorideHCID 219365771-(2,4-Difluoro-phenyl)-3-(2,2-dimethylpropyl)-thiourea

생성물 1

HCID 101496661-(2,4-Difluoro-phenyl)-3-(2,2-dimethyl-propyl)-2-thioxo-imidazolidine-4,5-dione수율 55%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Ethyl chlorooxoacetate (0.57 mL, 5.03 mmol) was added to a stirring solution of the above thiourea (1.00 g, 3.87 mmol) in dichloromethane (15 mL) and the resulting mixture was stirred overnight at room temperature. Concentration, trituration of the residue with diethyl ether, and recrystallization from boiling methanol afforded 0.66 g (55%) of 1-(2,4-difluoro-phenyl)-3-(2,2-dimethyl-propyl)-2-thioxo-imidazolidine-4,5-dione as a yellow solid: mp 156.2–156.9° C.; 1H NMR (DMSO-d6): δ 7.55 (m, 2H), 7.30 (m, 1H), 3.76 (m, 2H), 0.95 (s, 9H); IR (KBr): 3510 2920, 2230, 1775 cm1; MS (m/z) 312 (M+).

후처리

  1. concentrationConcentration, trituration of the residue
  2. customwith diethyl ether, and recrystallization

출처 및 근거

ORD 기록
ord-55306a01b4794eb3ba1ab7c822bd1ed8
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07115620B2

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