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Isoamyl Nitrite → 7-Chloro-2-methyl-3-nitrosoimidazo[2,1-a]isoquinoline

HRID 1788930
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인쇄 미리보기

반응식

HRID 1788930 반응식
[N:1](OCCC(C)C)=[O:2].[Cl:9][C:10]1[CH:19]=[CH:18][CH:17]=[C:16]2[C:11]=1[CH:12]=[CH:13][N:14]1[CH:22]=[C:21]([CH3:23])[N:20]=[C:15]12>O1CCOCC1>[Cl:9][C:10]1[CH:19]=[CH:18][CH:17]=[C:16]2[C:11]=1[CH:12]=[CH:13][N:14]1[C:22]([N:1]=[O:2])=[C:21]([CH3:23])[N:20]=[C:15]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8053Isoamyl NitriteHCID 138218267-Chloro-2-methylimidazo[2,1-a]isoquinoline

생성물 1

HCID 138218497-Chloro-2-methyl-3-nitrosoimidazo[2,1-a]isoquinoline수율 39.7%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Isoamyl nitrite (140 g) was added to a suspension of 7-chloro-2-methylimidazo[2,1-a]isoquinoline (17.1 g) in dioxane (170 ml) at 50° C. and the mixture was refluxed for 15 minutes. After being cooled, the resulting precipitate was collected by filtration, washed successively with dioxane and diethyl ether and dried in a desiccator to give 7-chloro-2-methyl-3-nitrosoimidazo[2,1-a]isoquinoline (7.7 g).

후처리

  1. temperaturethe mixture was refluxed for 15 minutes
  2. temperatureAfter being cooled
  3. filtrationthe resulting precipitate was collected by filtration
  4. washwashed successively with dioxane and diethyl ether
  5. customdried in a desiccator

출처 및 근거

ORD 기록
ord-bad33391a14d457ea99c0d986f93938b
출처 데이터셋
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04686227

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