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Triethylamine → 5-Chloro-2-methoxyphenyl-1-methyl-2-thioxo-imidazolidin-4-one

HRID 742227
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인쇄 미리보기

반응식

HRID 742227 반응식
Cl.C([O:4][C:5](=O)[CH2:6][NH:7][CH3:8])C.[Cl:10][C:11]1[CH:12]=[CH:13][C:14]([O:20][CH3:21])=[C:15]([N:17]=[C:18]=[S:19])[CH:16]=1.C(N(CC)CC)C>C(Cl)(Cl)Cl>[Cl:10][C:11]1[CH:12]=[CH:13][C:14]([O:20][CH3:21])=[C:15]([N:17]2[C:5](=[O:4])[CH2:6][N:7]([CH3:8])[C:18]2=[S:19])[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 171173Ethyl N-methylaminoacetate hydrochlorideHCID 7371654-Chloro-2-isothiocyanato-1-methoxy-benzene

생성물 1

HCID 190697455-Chloro-2-methoxyphenyl-1-methyl-2-thioxo-imidazolidin-4-one수율 87.2%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A mixture of sarcosine ethyl ester hydrochloride (7.68 g), 5-chloro-2-methoxyphenyl-isothiocyanate (10.0 g), triethylamine (10.0 g) and chloroform (150 mL) was heated at reflux for 4.5 hours. The mixture was cooled to ambient temperature. The precipitated solid was collected, washed with chloroform and air dried to give the title compound (11.8 g) as an off-white solid, m.p. 245°-247° C. Anal. Calcd. for C11H11Cl N2O S: C, 48.80; H, 4.10; N,10.35. Found: C, 48.42; H, 3.96; N, 10.33. Mass spectrum (El, M.+) m/z 270.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 4.5 hours
  3. customThe precipitated solid was collected
  4. washwashed with chloroform and air
  5. customdried

출처 및 근거

ORD 기록
ord-439962a4409046cf9808ce03d0c5b20e
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05554607

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