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HCID 57912454, 화합물 → 3-[2,6-Dimethoxy-4-(methoxymethyl)phenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazole-7-amine

HRID 1971782
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HRID 1971782 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][O:10][CH3:11])[CH:6]=[C:5]([O:12][CH3:13])[C:4]=1[C:14]1[N:15]2[N:21]=[C:20]([O:22][CH3:23])[C:19]([N:24]=O)=[C:16]2[S:17][CH:18]=1>[C].[Pd].C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][O:10][CH3:11])[CH:6]=[C:5]([O:12][CH3:13])[C:4]=1[C:14]1[N:15]2[N:21]=[C:20]([O:22][CH3:23])[C:19]([NH2:24])=[C:16]2[S:17][CH:18]=1
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참가 물질

4

반응물 1

HCID 57912454HCID 57912454, 화합물

생성물 1

HCID 579124433-[2,6-Dimethoxy-4-(methoxymethyl)phenyl]-6-methoxypyrazolo[5,1-b][1,3]thiazole-7-amine수율 63.5%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 8857Ethyl Acetate용매

실험 절차

Ethyl acetate (109 mL) and 10% palladium-carbon powder (50% wet: 2.34 g, 2.2 mmol) were added in that order to 3-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-6-methoxy-7-nitrosopyrazolo[5,1-b][1,3]thiazole (2.34 g, 6.44 mmol), and the mixture was stirred for 1 hour under a hydrogen atmosphere. The mixture was filtered with Celite and the solvent in the obtained filtrate was distilled off under reduced pressure. The residue was purified by (NH)silica gel column chromatography (ethyl acetate) to obtain the title compound (1.43 g, 4.09 mmol).

후처리

  1. filtrationThe mixture was filtered with Celite
  2. distillationthe solvent in the obtained filtrate was distilled off under reduced pressure
  3. customThe residue was purified by (NH)silica gel column chromatography (ethyl acetate)

출처 및 근거

ORD 기록
ord-3c91d05d861e474490c8609c92888aba
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431603B2

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