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Ethanethiol → HCID 19083168, 화합물

HRID 1378927
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HRID 1378927 반응식
[CH2:1]([SH:3])[CH3:2].CC(C)([O-])C.[K+].F[C:11]1[C:12]2[C:16]([CH:17]=[CH:18][CH:19]=1)=[N:15][N:14]([CH3:20])[C:13]=2[S:21]([NH2:24])(=[O:23])=[O:22]>CS(C)=O>[CH2:1]([S:3][C:11]1[C:12]2[C:16]([CH:17]=[CH:18][CH:19]=1)=[N:15][N:14]([CH3:20])[C:13]=2[S:21]([NH2:24])(=[O:23])=[O:22])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6343EthanethiolHCID 190831614-fluoro-2-methyl-2H-indazole-3-sulfonamideHCID 23665647Potassium tert-butoxide

생성물 1

HCID 19083168HCID 19083168, 화합물수율 72.5%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

반응 조건

온도
120 °C

실험 절차

4.8 g (77 mmol) of ethanethiol was added to a solution containing 8.6 g (77 mmol) of potassium t-butoxide in DMSO (70 ml), under cooling with ice, and 8 g (35 mmol) of 4-fluoro-2-methyl-2H-indazole-3-sulfonamide was further added thereto. This mixture was stirred at 120° C. for 2 hours. After confirming the disappearance of the starting material by TLC, treatment was conducted in the same manner as in Preparation Example 6 to obtain 6.8 g (yield: 72.5%) of the desired product. Melting: 145°-147° C.

후처리

  1. additionwas further added
  2. customwas conducted in the same manner as in Preparation Example 6

출처 및 근거

ORD 기록
ord-b322c3eda6de4461ae55a9485f913b57
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670452

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