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Water → HCID 17747837, 화합물

HRID 555956
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HRID 555956 반응식
[F:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([CH3:8])[C:3]=1[C:9]([NH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18]([OH:24])([CH3:23])[CH2:19][CH:20]([CH3:22])[CH3:21])=O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O>C1(C)C=CC=CC=1>[F:1][C:2]1[N:6]([CH3:7])[N:5]=[C:4]([CH3:8])[C:3]=1[C:9]1[O:24][C:18]([CH2:19][CH:20]([CH3:21])[CH3:22])([CH3:23])[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[N:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 17747836HCID 17747836, 화합물

생성물 1

HCID 17747837HCID 17747837, 화합물수율 63%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

The above product from step 2 is boiled in 150 ml of toluene with 0.2 g of p-toluenesulphonic acid on a water separator for 2 h. The mixture is washed with aqueous sodium bicarbonate solution and the organic phase is concentrated under reduced pressure. By stirring with heptane, it is possible to precipitate and remove by filtration the N-(2-acetylphenyl)-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide still present from the previous step. Chromatography gives 7.2 g (purity 85.1%; 63% of theory) of 2-(5-fluoro-1,3-dimethyl-1H-pyrazol-4-yl)-4-isobutyl-4-methyl-4H-3,1-benzoxazine.

후처리

  1. washThe mixture is washed with aqueous sodium bicarbonate solution
  2. concentrationthe organic phase is concentrated under reduced pressure
  3. customto precipitate
  4. customremove by filtration the N-(2-acetylphenyl)-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide

출처 및 근거

ORD 기록
ord-7bf960937c0d410cac83907d809ce0e3
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053572B2

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