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Dimethylamine → HCID 20309703, 화합물

HRID 437378
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인쇄 미리보기

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HRID 437378 반응식
[NH2:1][C:2]1[C:3]([I:18])=[C:4]([C:8]([I:17])=[C:9]([N:12]([CH3:16])[C:13](=[O:15])[CH3:14])[C:10]=1[I:11])[C:5]([OH:7])=O.S(Cl)(Cl)=O.[CH3:23][NH:24][CH3:25].[OH-].[Na+]>O>[NH2:1][C:2]1[C:3]([I:18])=[C:4]([C:8]([I:17])=[C:9]([N:12]([CH3:16])[C:13](=[O:15])[CH3:14])[C:10]=1[I:11])[C:5]([N:24]([CH3:25])[CH3:23])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 674DimethylamineHCID 14798Sodium HydroxideHCID 24386Thionyl ChlorideHCID 203096823-amino-2,4,6-triiodo-5-(N-methylacetamido)benzoic acid

생성물 1

HCID 20309703HCID 20309703, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

The acid chloride (16.23 g.) prepared from 3-amino-5-(N-methylacetamido)-2,4,6-triiodobenzoic acid and thionyl chloride was interacted with 60 ml. of dimethylamine (40% in water), 20 ml. of 35% aqueous sodium hydroxide and 30 ml. of water. The product was isolated and recrystallized from isopropyl alcohol to give 3-amino-2,4,6-triiodo-5-(N-methylacetamido)N,N-dimethylbenzamide as a pale yellow solid, m.p. 235°-240° C.

후처리

  1. customThe product was isolated
  2. customrecrystallized from isopropyl alcohol

출처 및 근거

ORD 기록
ord-97f9e1f566a7425d9e6dfe600a6e5611
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04031088

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