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Methane → HCID 178449901, 화합물

HRID 2071890
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HRID 2071890 반응식
[CH2:1]([NH:5][C:6](=[NH:8])[CH3:7])[CH2:2][CH2:3][CH3:4].[N+:9](=[C:11]1[N:15]=[N:14][N:13]=[C:12]1[C:16]([NH2:18])=[O:17])=[N-:10].C>C(O)C>[CH2:1]([N:5]([C:6](=[NH:8])[CH3:7])[N:10]=[N:9][C:11]1[NH:15][N:14]=[N:13][C:12]=1[C:16]([NH2:18])=[O:17])[CH2:2][CH2:3][CH3:4]
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참가 물질

5

반응물 3

HCID 297MethaneHCID 54301235Amino(5-diazonio-4H-1,2,3-triazol-4-ylidene)methanolateHCID 178449087HCID 178449087, 화합물

생성물 1

HCID 178449901HCID 178449901, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

5.7 g. of N-butyl-acetamidine are dissolved in 300 ml of anhydrous ethanol, whereupon 7 g. of 5-diazo-1,2,3-triazole-4-carboxamide are added at 25° C. within half an hour. After 3 hours the solution is clarified with activated charcoal and evaporated in vacuo. The residual thick oil is admixed with 40 ml of anhydrous ethylacetate and the crude product (9.7 g. melting at 150° C. decomposition) is recrystallized from a mixture of 110 ml of acetone and 40 ml of anhydrous ethanol. Thus 6.1 g. of 5-[3-n-butyl-3-(alpha-iminoethyl)-1-triazeno]-1,2,3-triazole-4-carboxamide melting at 159°-160° C. (decomposition) are obtained.

후처리

  1. customevaporated in vacuo
  2. customthe crude product (9.7 g. melting at 150° C. decomposition) is recrystallized from a mixture of 110 ml of acetone and 40 ml of anhydrous ethanol

출처 및 근거

ORD 기록
ord-8de3f4085d3f46a4885e2c7d04e01d28
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04049639

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