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HCID 68754553, 화합물 → 5-Amino-4-(thiazol-2-yl)thiophene-3-carbonitrile

HRID 2098134
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HRID 2098134 반응식
[N+:1]([C:4]1[S:8][CH:7]=[C:6]([C:9]#[N:10])[C:5]=1[C:11]1[S:12][CH:13]=[CH:14][N:15]=1)([O-])=O>[Fe].CC(O)=O>[NH2:1][C:4]1[S:8][CH:7]=[C:6]([C:9]#[N:10])[C:5]=1[C:11]1[S:12][CH:13]=[CH:14][N:15]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68754553HCID 68754553, 화합물

생성물 1

HCID 687563605-Amino-4-(thiazol-2-yl)thiophene-3-carbonitrile

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

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온도
60 °C

실험 절차

A 30 mL reaction vial was charged with 5-nitro-4-(thiazol-2-yl)thiophene-3-carbonitrile (180 mg, 0.76 mmol) and AcOH (3 mL). A spatula tip of iron dust was added and the reaction vial was heated to 60° C. for 20 min. The reaction mixture was cooled to 23° C. and partitioned between methylene chloride and sodium bicarbonate solution. The organic solution was dried over sodium sulfate and concentrated to give 5-amino-4-(thiazol-2-yl)thiophene-3-carbonitrile as a red solid. LCMS showed an m/z of 208.0 with a retention time of 2.016 min using method [1].

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후처리

  1. customA 30 mL reaction
  2. customthe reaction
  3. temperatureThe reaction mixture was cooled to 23° C.
  4. custompartitioned between methylene chloride and sodium bicarbonate solution
  5. dry with materialThe organic solution was dried over sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8723a58741f3407282de5ec0659850f0
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450363B2

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