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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethylamine → N-(4-bromo-1,3-thiazol-5-yl)acetamide

HRID 1051417
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HRID 1051417 반응식
Br[C:2]1[S:3][C:4]([NH:8][C:9](=[O:11])[CH3:10])=[C:5]([Br:7])[N:6]=1.C(NCC)C>C(O)C.[Ni]>[Br:7][C:5]1[N:6]=[CH:2][S:3][C:4]=1[NH:8][C:9](=[O:11])[CH3:10]
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참가 물질

5

반응물 2

HCID 8021DiethylamineHCID 86715553N-(2,4-dibromothiazol-5-yl)acetamide

생성물 1

HCID 83680500N-(4-bromo-1,3-thiazol-5-yl)acetamide수율 78%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 702Ethanol용매

실험 절차

A mixture of N-(2,4-dibromothiazol-5-yl)acetamide from example 1.4 (0.35 g, 1.17 mmol), diethylamine (0.085 g, 1.17 mmol) and Raney Ni (0.14 g, 2.33 mmol) in ethanol (50 mL) was stirred at room temperature for 12 h in a 100 mL round-bottomed flask to give a black solution. The reaction mixture was filtered and concentrated to give the title compound (0.20 g, 0.91 mmol, 78%) as a yellow solid which was directly used for the next step without purification.

후처리

  1. customto give a black solution
  2. filtrationThe reaction mixture was filtered
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-20f70f9f594f4f83b1277f2452573fc9
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388180B2

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