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2-Azido-3-(4-bromo-5-methyl-thiophen-2-yl)-acrylic acid methyl ester → methyl 3-bromo-2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate

HRID 1951639
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인쇄 미리보기

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HRID 1951639 반응식
[CH3:1][O:2][C:3](=[O:16])[C:4]([N:13]=[N+]=[N-])=[CH:5][C:6]1[S:7][C:8]([CH3:12])=[C:9]([Br:11])[CH:10]=1>C1(C)C(C)=CC=CC=1>[CH3:1][O:2][C:3]([C:4]1[NH:13][C:10]2[C:9]([Br:11])=[C:8]([CH3:12])[S:7][C:6]=2[CH:5]=1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 767450662-Azido-3-(4-bromo-5-methyl-thiophen-2-yl)-acrylic acid methyl ester

생성물 1

HCID 12025193methyl 3-bromo-2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate수율 76.5%

시약·촉매·용매 1

HCID 7237O-Xylene용매2회

실험 절차

To a refluxing xylene (100 ml) was added the crude product of Step 2 (18 g) in 250 ml of xylene over a period of 20 min. After refluxing for 10 min, the reaction mixture was cooled and concentrated to volume of about 100 ml. The solid was collected by filtration to give 12.5 g of the title compound as a white solid.

후처리

  1. temperatureAfter refluxing for 10 min
  2. temperaturethe reaction mixture was cooled
  3. concentrationconcentrated to volume of about 100 ml
  4. filtrationThe solid was collected by filtration

출처 및 근거

ORD 기록
ord-1920b700faca484098975edb2fd6cc41
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08404736B2

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