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Hydrogen Peroxide → HCID 178433361, 화합물

HRID 1710814
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HRID 1710814 반응식
I.[Cl:2][C:3]1[CH:12]=[CH:11][C:10]([Cl:13])=[C:9]2[C:4]=1[CH:5]([CH3:16])[NH:6][C:7](SC)=[N:8]2.[OH-].[NH4+:18].[OH-].[Na+].OO>C(#N)C.O>[Cl:2][C:3]1[CH:12]=[CH:11][C:10]([Cl:13])=[C:9]2[C:4]=1[CH:5]([CH3:16])[NH:6][C:7]([NH2:18])=[N:8]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 14923Ammonium HydroxideHCID 178503353HCID 178503353, 화합물

생성물 1

HCID 178433361HCID 178433361, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 6342
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
Acetonitrile
용매

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온도
170 °C

실험 절차

5,8-Dichloro-4-methyl-2-methylsulfanyl-3,4-dihydro-quinazoline hydroiodide (116 mg, 0.30 mmol) was suspended in a mixture of ammonium hydroxide (0.22 ml, 25% in H2O, 3 mmol) and acetonitrile (0.9 ml), and heated in a microwave oven to 170° C. (30 min). The reaction was cooled in an ice bath and treated with 1N aqueous sodium hydroxide solution (0.9 ml) and 5-6 drops of concentrated solution of aqueous hydrogen peroxide. A little water was added, and the title compound (36 mg, 52%) was filtered off as a white solid.

후처리

  1. temperatureThe reaction was cooled in an ice bath
  2. filtrationthe title compound (36 mg, 52%) was filtered off as a white solid

출처 및 근거

ORD 기록
ord-a52f4ed69a72466d8c2d477b4f28c55f
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790732B2

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