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Hydrochloric Acid → 2-[3-(3-Iodophenyl)-2,4-dioxoimidazolidin-1-yl]acetamide

HRID 857122
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HRID 857122 반응식
[I:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12](=[O:13])[CH2:11][NH:10][C:9]2=[O:14])[CH:5]=[CH:6][CH:7]=1.[H-].[Na+].Br[CH2:18][C:19]([NH2:21])=[O:20].Cl>CN(C=O)C>[I:1][C:2]1[CH:3]=[C:4]([N:8]2[C:12](=[O:13])[CH2:11][N:10]([CH2:18][C:19]([NH2:21])=[O:20])[C:9]2=[O:14])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 696322-BromoacetamideHCID 218671043-(3-Iodophenyl)imidazolidine-2,4-dione

생성물 1

HCID 218671362-[3-(3-Iodophenyl)-2,4-dioxoimidazolidin-1-yl]acetamide수율 53.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide
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용매

실험 절차

A solution of 3-(3-iodophenyl)imidazolidine-2,4-dione (1 g) in DMF (20 ml) was treated with sodium hydride (60% oil dispersion, 158 mg) and 2-bromoacetamide (1.36 g) at 20° C. After 2 h the reaction mixture was treated with aqueous 2M HCl, extracted with EtOAc and dried (MgSO4). The solvent was removed under reduced pressure and the residue was purified by chromatography on Biotage (40 g) eluting with EtOAc to give the title compound (638 mg). LCMS RT=2.32 min.

후처리

  1. extractionextracted with EtOAc
  2. dry with materialdried (MgSO4)
  3. customThe solvent was removed under reduced pressure
  4. customthe residue was purified by chromatography on Biotage (40 g)
  5. washeluting with EtOAc

출처 및 근거

ORD 기록
ord-0253ce75f86c4ad0ba150c9855cc5e5d
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07144908B2

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