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3-Amino-5-(4-fluorophenyl)thiophene-2-carboxamide → 3-[(Aminocarbonyl)amino]-5-(4-fluorophenyl)-2-thiophenecarboxamide

HRID 900418
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인쇄 미리보기

반응식

HRID 900418 반응식
[N-:1]=[C:2]=[O:3].[Na+].[NH2:5][C:6]1[CH:10]=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[S:8][C:7]=1[C:18]([NH2:20])=[O:19]>C(O)(=O)C.O>[NH2:1][C:2]([NH:5][C:6]1[CH:10]=[C:9]([C:11]2[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=2)[S:8][C:7]=1[C:18]([NH2:20])=[O:19])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 27829033-Amino-5-(4-fluorophenyl)thiophene-2-carboxamideHCID 11051568NaNCO

생성물 1

HCID 98171243-[(Aminocarbonyl)amino]-5-(4-fluorophenyl)-2-thiophenecarboxamide수율 13.2%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

Sodium isocyanate (1.08 g) was added portionwise to a stirred suspension of 3-amino-5-(4-fluorophenyl)-2-thiophenecarboxamide (3.2 g) in acetic acid (150 mL) and water (90 mL). After 20 h, the solid was filtered off and washed with water, methanol and ether. Recrystallisation from methanol/dimethylsulphoxide gave the title urea (0.5 g) as a 1:1 dimethylsulphoxide solvate.

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후처리

  1. filtrationthe solid was filtered off
  2. washwashed with water, methanol and ether
  3. customRecrystallisation from methanol/dimethylsulphoxide

출처 및 근거

ORD 기록
ord-980b78b90efd4c4692f839fc19df05d9
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07358376B2

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