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methyl 3-isothiocyanato-4-methylthiophene-2-carboxylate → HCID 178431853, 화합물

HRID 574733
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인쇄 미리보기

반응식

HRID 574733 반응식
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([NH2:10])=[CH:9][C:4]=2[N:3]=[CH:2]1.[N:11]([C:14]1[C:18]([CH3:19])=[CH:17][S:16][C:15]=1[C:20](OC)=[O:21])=[C:12]=[S:13]>C1COCC1>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([N:10]3[C:20](=[O:21])[C:15]4[S:16][CH:17]=[C:18]([CH3:19])[C:14]=4[NH:11][C:12]3=[S:13])=[CH:9][C:4]=2[N:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2777569methyl 3-isothiocyanato-4-methylthiophene-2-carboxylateHCID 178507353HCID 178507353, 화합물

생성물 1

HCID 178431853HCID 178431853, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

1H-benzo[d]imidazol-5-amine (0.13 g, 0.98 mmol) and methyl 3-isothiocyanato-4-methylthiophene-2-carboxylate (0.21 g, 0.98 mmol) were dissolved in 10 mL of THF. The mixture was stirred by heating under reflux over night. The solvent was removed and the product was purified by means of semi-preparative HPLC.

후처리

  1. temperatureby heating
  2. temperatureunder reflux over night
  3. customThe solvent was removed
  4. customthe product was purified by means of semi-preparative HPLC

출처 및 근거

ORD 기록
ord-ee12f5ef980c4ddd8587512812870033
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09034907B2

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