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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(2-Amino-1,3-thiazol-4-yl)acetamide → 4-Thiazoleacetonitrile, 2-amino-

HRID 1872011
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인쇄 미리보기

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HRID 1872011 반응식
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([CH2:7][C:8]([NH2:10])=O)[N:6]=1>P(Cl)(Cl)(Cl)=O>[NH2:1][C:2]1[S:3][CH:4]=[C:5]([CH2:7][C:8]#[N:10])[N:6]=1
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참가 물질

3

반응물 1

HCID 70640912-(2-Amino-1,3-thiazol-4-yl)acetamide

생성물 1

HCID 186897514-Thiazoleacetonitrile, 2-amino-

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

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온도
90 °C

실험 절차

A mixture of the product from step (i) (9.5 g) and phosphorous oxychloride (30 ml) was heated at 90° C. for 2 hours. The mixture was evaporated under reduced pressure and poured onto a mixture of ice water and ethyl acetate. The aqueous phase was adjusted to pH 9 with sodium bicarbonate and extracted repeatedly with ethyl acetate. The combined extract was dried (MgSO4) and evaporated. The residue was purified by chromatography eluting with ethyl acetate. Yield 6.1 g. 1H NMR: δ (DMSO) 7.08(br s,2H), 6.40(s,1H), 3.77(s,2H).

후처리

  1. customThe mixture was evaporated under reduced pressure
  2. additionpoured onto a mixture of ice water and ethyl acetate
  3. extractionextracted repeatedly with ethyl acetate
  4. extractionThe combined extract
  5. dry with materialwas dried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by chromatography
  8. washeluting with ethyl acetate

출처 및 근거

ORD 기록
ord-d0ad4b5a45564d7898a3883e7bdd7a32
출처 데이터셋
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06107297

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