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Hydrogen Sulfide → HCID 12831166, 화합물

HRID 2285592
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HRID 2285592 반응식
[SH2:1].[NH2:2][C:3]1[C:8]([C:9]#[N:10])=[CH:7][N:6]=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:4]=1.O>N1C=CC=CC=1>[NH2:2][C:3]1[C:8]([C:9](=[S:1])[NH2:10])=[CH:7][N:6]=[C:5]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 402Hydrogen SulfideHCID 962WaterHCID 128311604-Amino-2-phenylpyrimidine-5-carbonitrile

생성물 1

HCID 12831166HCID 12831166, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Hydrogen sulfide is passed through a solution of 4-amino-2-phenyl-5-pyrimidinecarbonitrile (9.811 g., 0.050 mole) in dry pyridine (125 ml.) for one hour. The emerald green solution is stored overnight at 5° C. The solution is poured into water (500 ml.) with stirring. After stirring for one hour at ambient temperature, the pale yellow solid which separated is collected by filtration, dried at 110° C./0.1 mm. The yield of product melting at 197° C. dec. (uncorr.) was 10.481 g. (91.0%). The initial product is recrystallized from toluene (Darco G-60) affording yellow needles melting at 198° C. dec. (uncorr.) in a yield of 7.733 g. (67.1%).

후처리

  1. stirringAfter stirring for one hour at ambient temperature
  2. customthe pale yellow solid which separated
  3. filtrationis collected by filtration
  4. customdried at 110° C./0.1 mm
  5. customThe initial product is recrystallized from toluene (Darco G-60)

출처 및 근거

ORD 기록
ord-15e216c3faad4b32a438bf07bef8c903
출처 데이터셋
uspto-grants-1982_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04323681

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