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Dimethylformamide dimethyl acetal → HCID 136000308, 화합물

HRID 1378932
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인쇄 미리보기

반응식

HRID 1378932 반응식
CO[CH:3](OC)[N:4]([CH3:6])[CH3:5].[OH:9][C:10]1[C:11]2[C:15]([CH:16]=[CH:17][CH:18]=1)=[N:14][N:13]([CH3:19])[C:12]=2[S:20]([NH2:23])(=[O:22])=[O:21]>C(#N)C>[CH3:6][N:4]([CH3:5])[CH:3]=[N:23][S:20]([C:12]1[N:13]([CH3:19])[N:14]=[C:15]2[C:11]=1[C:10]([OH:9])=[CH:18][CH:17]=[CH:16]2)(=[O:21])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 135829371HCID 135829371, 화합물

생성물 1

HCID 136000308HCID 136000308, 화합물수율 86.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

21.3 g (174 mmol) of dimethylformamide dimethylacetal was dropwise added to a solution containing 33 g (145 mmol) of 4-hydroxy-2-methyl-2H-indazole-3-sulfonamide in 200 ml of acetonitrile, at room temperature. The mixture was stirred for one hour, then poured into ice water and extracted with ethyl acetate. The organic layer was washed with water, then concentrated and purified by column chromatography to obtain 35.2 g (yield: 86.3%) of the desired product. Melting point: 118°-119° C.

후처리

  1. customat room temperature
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. concentrationconcentrated
  5. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-2117faa0648b4e4da70bf5e77d15a053
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670452

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