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Diethyl Ether → HCID 13178507, 화합물

HRID 1981443
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HRID 1981443 반응식
[C:1]([C:4]1[CH:9]=[C:8]([Br:10])[C:7]([OH:11])=[C:6]([Br:12])[CH:5]=1)(=[NH:3])[NH2:2].[CH2:13](Cl)[C:14]1[CH:22]=[CH:21][C:20]2[O:19][CH2:18][O:17][C:16]=2[CH:15]=1.C([O:26]CC)C>N1C=CC=CC=1>[CH2:18]1[O:19][C:20]2[CH:21]=[CH:22][C:14]([C:13]([O:11][C:7]3[C:6]([Br:12])=[CH:5][C:4]([C:1](=[NH:2])[NH2:3])=[CH:9][C:8]=3[Br:10])=[O:26])=[CH:15][C:16]=2[O:17]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 887131,3-Benzodioxole, 5-(chloromethyl)-HCID 42288753,5-Dibromo-4-hydroxy-benzamidine

생성물 1

HCID 13178507HCID 13178507, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 5 g of 4-amidino-2,6-dibromophenol in 100 ml of pyridine, while being cooled in ice and stirred, was added 2.4 g of piperonyl chloride. The mixture was stirred for 30 minutes while being cooled in ice, then for 3 hours at room temperature, and mixed with about 300 cc of ethyl ether. The precipitate which was formed was collected by filtration and recrystallized from ethanol to obtain 4.8 g of colorless crystals of 4-amidino-2,6-dibromophenyl 3,4-methylenedioxybenzoate methanesulfonate.

후처리

  1. stirringThe mixture was stirred for 30 minutes
  2. temperaturewhile being cooled in ice
  3. customThe precipitate which was formed
  4. filtrationwas collected by filtration
  5. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-58a13f7ca8d64029b49f866f95c58af4
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04514416

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