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Methyl 3-amino-2-thiophenecarboxylate → HCID 5178717, 화합물

HRID 902501
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HRID 902501 반응식
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1[NH2:10])=[O:4]>C(CC(OC)=O)#N>[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1[NH:10][C:3](=[O:2])[CH2:5][C:9]#[N:10])=[O:4]
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참가 물질

3

반응물 1

HCID 89652Methyl 3-amino-2-thiophenecarboxylate

생성물 1

HCID 5178717HCID 5178717, 화합물수율 100.3%

시약·촉매·용매 1

HCID 7747Methyl cyanoacetate용매

실험 절차

A solution of methyl-3-amino-thiophene-2-carboxylate (13 g, 82.70 mmol) in neat methyl cyanoacetate (40 mL) was heated at 210° C. for 10 h. The solution was cooled and excess methyl cyanoacetate was distilled off under vacuum. The residue was taken in methanol, sonicated briefly, and filtered. The solids were washed by cold methanol and dried to yield 9.3 g (50%) of 3-(2-cyano-acetylamino)-thiophene-2-carboxylic acid methyl ester as white solids. MP 146° C.; 1H NMR (400 MHz, DMSO-d6) δ 4.18 (s, 2H), 7.86 (d, J=5.2 Hz, 1H), 7.93 (d, J=5.2 Hz, 1H), 10.25 (s, 1H) ppm; MS m/z=225 amu (M++1).

후처리

  1. temperatureThe solution was cooled
  2. distillationexcess methyl cyanoacetate was distilled off under vacuum
  3. customsonicated briefly
  4. filtrationfiltered
  5. washThe solids were washed by cold methanol
  6. customdried

출처 및 근거

ORD 기록
ord-d744d1e5b27446b5b3e6125be36e4561
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365200B2

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