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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aziridine-2-carbonitrile → HCID 21161947, 화합물

HRID 893956
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HRID 893956 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([N:8]=[C:9]=[O:10])=[O:7].[C:11]([CH:13]1[CH2:15][NH:14]1)#[N:12]>C1(C)C=CC=CC=1>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([NH:8][C:9]([N:14]1[CH2:15][CH:13]1[C:11]#[N:12])=[O:10])=[O:7]
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참가 물질

4

반응물 2

HCID 118115Aziridine-2-carbonitrileHCID 126085392-Thiophenecarbonyl isocyanate

생성물 1

HCID 21161947HCID 21161947, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매2회

실험 절차

2.76 g. Thiophene-2-carbonyl isocyanate are dissolved in 45 ml. anhydrous toluene and mixed dropwise, while stirring, at 20° to 30° C. with a solution of 1.22 g. 2-cyanoaziridine in 30 ml. toluene. Stirring is continued for 1 hour at ambient temperature and the precipitate obtained is filtered off with suction, washed with toluene and subsequently triturated with diethyl ether. There are thus obtained 3.4 g. 1-(N-2-thiophene-carbonyl-carbamoyl)-2-cyanoaziridine; m.p. 156°-160° C., which still contains a little thiophene-2-carboxylic acid amide.

후처리

  1. stirringStirring
  2. customthe precipitate obtained
  3. filtrationis filtered off with suction
  4. washwashed with toluene
  5. customsubsequently triturated with diethyl ether

출처 및 근거

ORD 기록
ord-86125920b2814ee88f415d6ae0b6b6b5
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04282212

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