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Ethanol → HCID 178457088, 화합물

HRID 1189667
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HRID 1189667 반응식
[F:1][C:2]([F:29])([F:28])[C@H:3]1[CH2:8][CH2:7][C@H:6]([NH:9][C:10](=[O:27])[C:11]2[CH:16]=[C:15]([N+:17]([O-])=O)[C:14]([NH:20][CH3:21])=[CH:13][C:12]=2[N:22]([CH3:26])[CH2:23][C:24]#[CH:25])[CH2:5][CH2:4]1.[O-]S(S([O-])=O)=O.[Na+].[Na+].O.CCO>C([O-])(O)=O.[Na+]>[F:1][C:2]([F:28])([F:29])[C@H:3]1[CH2:8][CH2:7][C@H:6]([NH:9][C:10](=[O:27])[C:11]2[CH:16]=[C:15]([NH2:17])[C:14]([NH:20][CH3:21])=[CH:13][C:12]=2[N:22]([CH3:26])[CH2:23][C:24]#[CH:25])[CH2:5][CH2:4]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702EthanolHCID 962WaterHCID 24489Sodium DithioniteHCID 178457089HCID 178457089, 화합물

생성물 1

HCID 178457088HCID 178457088, 화합물

시약·촉매·용매 1

HCID 516892Sodium Bicarbonate용매

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온도
55 °C

실험 절차

A mixture of N-(trans-4-trifluoromethyl-cyclohexyl)-2-[N-methyl-N-propargylamino]-4-methylamino-5-nitro-benzoic acid amide (60 mg, 0.145 mmol), Na2S2O4 (127 mg and a second 150 mg portion is added after 8 h), 1 mL water and 5 mL EtOH is stirred at 55° C. for 24 h. The mixture is diluted with sat aq NaHCO3 and extracted with EtOAc. The combined organic phases are dried with Na2SO4, filtered and concentrated.

후처리

  1. extractionextracted with EtOAc
  2. dry with materialThe combined organic phases are dried with Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-cf781453221e4dba93c905e764772c02
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08674113B2

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