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Hydrogen Sulfide → HCID 14579136, 화합물

HRID 2248359
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반응식

HRID 2248359 반응식
[SH2:1].C(O)C.[C:5]([CH:7]([C:17]1[O:18][CH:19]=[CH:20][CH:21]=1)[NH:8][C:9]([C:11]1[CH:12]=[N:13][N:14]([CH3:16])[CH:15]=1)=[O:10])#[N:6]>C(N(CC)CC)C>[O:18]1[CH:19]=[CH:20][CH:21]=[C:17]1[CH:7]([C:5](=[S:1])[NH2:6])[NH:8][C:9]([C:11]1[CH:12]=[N:13][N:14]([CH3:16])[CH:15]=1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 402Hydrogen SulfideHCID 702EthanolHCID 14579134HCID 14579134, 화합물

생성물 1

HCID 14579136HCID 14579136, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

Hydrogen sulfide was blown into an ethanol solution containing 1.4 g of the N-(cyano-2-furanylmethyl)-1-methyl-1H-pyrazol-4-carboxamide as obtained in the above process and 0.7 g of triethylamine, for 1 hour, and the whole was stirred for 1 hour under cooling with ice and then for a further 2 hours at room temperature. Afterwards, the crystal formed was taken out by filtration, washed with chloroform and then dried, to obtain 1.1 g of the intended N-[2-furanyl(thiocarbamoyl)-methyl]-1-methyl-1H-pyrazole-4-carboxamide.

후처리

  1. temperatureunder cooling with ice
  2. waitfor a further 2 hours at room temperature
  3. customAfterwards, the crystal formed
  4. filtrationwas taken out by filtration
  5. washwashed with chloroform
  6. customdried

출처 및 근거

ORD 기록
ord-c5dab063652b48cb84501c45d28f7ab9
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05039694

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