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Thiourea → HCID 178425296, 화합물

HRID 1027483
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인쇄 미리보기

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HRID 1027483 반응식
C[O-].[Na+].[NH2:4][C:5]([NH2:7])=[S:6].C([O:10][C:11](=O)[CH:12]([NH:18][C:19](=[O:27])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[CH:21]=1)[C:13](OCC)=[O:14])C>C(O)C>[OH:14][C:13]1[C:12]([NH:18][C:19](=[O:27])[C:20]2[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[CH:21]=2)=[C:11]([OH:10])[N:7]=[C:5]([SH:6])[N:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 2723790ThioureaHCID 10942334Sodium MethoxideHCID 33240476Diethyl 2-(3-methylbenzamido)malonate

생성물 1

HCID 178425296HCID 178425296, 화합물수율 100.8%

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
60 °C

실험 절차

1.5 equivalents of sodium methoxide (30% in methanol) were added to 7.79 g of thiourea in 150 ml of absolute ethanol. A solution of 30 g of 2-(3-methyl-benzoylamino)malonic acid diethyl ester in 100 ml of absolute ethanol was added dropwise, and the reaction mixture was stirred at 60° C. for 2 h. Then the mixture was cooled to 0° C. for 30 min, and the precipitate was filtered off with suction, washed and dried. 28.6 g of the crude title compound were obtained.

후처리

  1. temperatureThen the mixture was cooled to 0° C. for 30 min
  2. filtrationthe precipitate was filtered off with suction
  3. washwashed
  4. customdried

출처 및 근거

ORD 기록
ord-cb345fb32d0140bd88ee08a64e09f618
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735387B2

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