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Triethylamine → 3-(2-Chloro-4-methylphenyl)-1-ethyl-2-thioxo-imidazolidin-4-one

HRID 742255
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반응식

HRID 742255 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]=[C:10]=[S:11].[CH2:12]([NH:14][CH2:15][C:16](O)=[O:17])[CH3:13].C(N(CC)CC)C>C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[N:9]1[C:16](=[O:17])[CH2:15][N:14]([CH2:12][CH3:13])[C:10]1=[S:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 1435292-Chloro-4-methylphenyl isothiocyanateHCID 316542N-Ethylglycine

생성물 1

HCID 194253743-(2-Chloro-4-methylphenyl)-1-ethyl-2-thioxo-imidazolidin-4-one수율 21.7%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

The title compound was prepared by the procedure described in Example 28 using 18.3 g of 2-chloro-4-methylphenyl-isothiocyanate, 18.4 g of N-ethyl glycine, 20.2 g of triethyl amine, and 300 mL of chloroform. Crystallization from ethyl acetate afforded the title compound (5.8 g) as a peach solid, m.p. 126°-128° C. Anal. Calcd. for. C12H13Cl N2O S: C, 53.63; H, 4.88; N, 10.42. Found: C, 53.50; H, 4.76; N, 10.28. Mass spectrum (+FAB, IM+H]+) m/z 269/271.

후처리

  1. customThe title compound was prepared by the procedure
  2. customCrystallization from ethyl acetate

출처 및 근거

ORD 기록
ord-94fab187c7ba44d2a6cc0365d8243fc1
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05554607

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