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Isopropanol → 2-Chloro-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline

HRID 1900654
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인쇄 미리보기

반응식

HRID 1900654 반응식
C(O)(C)C.[CH2:5]([NH2:15])[C:6]1[CH:14]=[CH:13][C:12]2[O:11][CH2:10][O:9][C:8]=2[CH:7]=1.[Cl:16][C:17]1[N:26]=[C:25](Cl)[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([C:28]#[N:29])[CH:23]=2)[N:18]=1>C(N(CC)CC)C>[Cl:16][C:17]1[N:26]=[C:25]([NH:15][CH2:5][C:6]2[CH:14]=[CH:13][C:12]3[O:11][CH2:10][O:9][C:8]=3[CH:7]=2)[C:24]2[C:19](=[CH:20][CH:21]=[C:22]([C:28]#[N:29])[CH:23]=2)[N:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 75799Benzo-1,3-dioxole-5-methylamineHCID 187966702,4-Dichloroquinazoline-6-carbonitrile

생성물 1

HCID 211839842-Chloro-4-(3,4-methylenedioxybenzyl)amino-6-cyanoquinazoline수율 79.4%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

35 ml of isopropyl alcohol, 900 mg of triethylamine and 1.35 g of piperonylamine were added to 2 g of 2,4-dichloro-6-cyanoquinazoline. The obtained mixture was heated under reflux for 1.5 hours and hot-filtered to recover a precipitate. Thus, 2.4 g of the title compound was obtained.

후처리

  1. temperatureThe obtained mixture was heated
  2. temperatureunder reflux for 1.5 hours
  3. filtrationhot-filtered
  4. customto recover a precipitate

출처 및 근거

ORD 기록
ord-f297c731af234410b1c439d3668eb083
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05576322

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