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Toluene → HCID 69051761, 화합물

HRID 1784115
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HRID 1784115 반응식
S(O)(O)(=O)=O.[CH3:6][S:7][C:8]1[N:13]=[C:12]([NH2:14])[C:11]([NH2:15])=[C:10]([NH2:16])[N:9]=1.O.O.[Cl-:19].[Ba+2].[Cl-].C1(C)C=CC=CC=1>O>[ClH:19].[ClH:19].[NH2:16][C:10]1[C:11]([NH2:15])=[C:12]([NH2:14])[N:13]=[C:8]([S:7][CH3:6])[N:9]=1
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참가 물질

5

반응물 3

HCID 1140TolueneHCID 2292652-Methylsulfanylpyrimidine-4,5,6-triamine; sulfuric acidHCID 5284346Barium chloride, dihydrate

생성물 1

HCID 69051761HCID 69051761, 화합물수율 209.9%

시약·촉매·용매 1

HCID 962Water용매2회

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온도
80 °C

실험 절차

To a suspension of a 2-methylmercapto-4,5,6-triamino-pyrimidine sulfate (44.3 mmole), which may be prepared and characterised for instance as disclosed by Taylor et al. in J. Am. Chem. Soc. (1952) 74:1644-1647, in water (135 ml) at 80° C. was added dropwise a solution of barium chloride dihydrate (39.8 mmole) in water (25 ml). The suspension was stirred for 30 minutes at 80° C. The reaction mixture was cooled down and barium sulfate was filtered off over Celite. The filtrate was evaporated in vacuo and co-evaporated with toluene yielding the title compound as a yellow powder (10.2 g, 94% yield).

후처리

  1. custommay be prepared
  2. temperatureThe reaction mixture was cooled down
  3. filtrationbarium sulfate was filtered off over Celite

출처 및 근거

ORD 기록
ord-9cac5a6be1a440569a97960ad86d737e
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501513B2

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