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Water → HCID 58432990, 화합물

HRID 388420
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HRID 388420 반응식
[C:1]([O:5][C:6]([C:8]1[C:9]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)=[N:10][S:11][C:12]=1Br)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.C([O-])([O-])=O.[Na+].[Na+]>COCCOC>[C:1]([O:5][C:6]([C:8]1[C:9]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)=[N:10][S:11][C:12]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 10340Sodium CarbonateHCID 58432991HCID 58432991, 화합물

생성물 1

HCID 58432990HCID 58432990, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

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온도
100 °C

실험 절차

Starting material 9 (1.12 g) is dissolved in DME (12 ml) and to this are added 439 mg of 10, water (5 ml) and 954 mg of Na2CO3. The mixture is degassed with argon for 5 min. Pd(dppf)Cl2 (121 mg) is added, the tube is sealed and the reaction mixture is heated at 100° C. in the microwave for 15 min. TLC (Hep/EtOAc, 80/20) shows a good conversion into a slower moving spot. The reaction mixture is diluted with EtOAc and washed with water and brine. The organic layer is dried and concentrated. The residue is purified by flash column chromatography using 5% diisopropyl ether in heptane as eluent. Isothiazole 11 is obtained in good yield as a white crystalline solid.

후처리

  1. customThe mixture is degassed with argon for 5 min
  2. additionPd(dppf)Cl2 (121 mg) is added
  3. customthe tube is sealed
  4. additionThe reaction mixture is diluted with EtOAc
  5. washwashed with water and brine
  6. customThe organic layer is dried
  7. concentrationconcentrated
  8. customThe residue is purified by flash column chromatography

출처 및 근거

ORD 기록
ord-38de0480735640dc9bfc82ce695daaf3
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377953B2

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