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Chlorosuccinimide → 1-(4-Hydroxy-3-(hydroxymethyl)-1-butyl)-5-(1-azido-2-chloroethyl)uracil

HRID 732924
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HRID 732924 반응식
[Cl:1]N1C(=O)CCC1=O.[OH:9][CH2:10][CH:11]([CH2:24][OH:25])[CH2:12][CH2:13][N:14]1[CH:21]=[C:20]([CH:22]=[CH2:23])[C:18](=[O:19])[NH:17][C:15]1=[O:16].[N-:26]=[N+:27]=[N-:28].[Na+]>COCCOC.O>[OH:9][CH2:10][CH:11]([CH2:24][OH:25])[CH2:12][CH2:13][N:14]1[CH:21]=[C:20]([CH:22]([N:26]=[N+:27]=[N-:28])[CH2:23][Cl:1])[C:18](=[O:19])[NH:17][C:15]1=[O:16]
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참가 물질

6

반응물 3

HCID 31398ChlorosuccinimideHCID 33557Sodium AzideHCID 100372831-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracil

생성물 1

HCID 4903871-(4-Hydroxy-3-(hydroxymethyl)-1-butyl)-5-(1-azido-2-chloroethyl)uracil수율 47%

시약·촉매·용매 2

HCID 962Water용매
HCID 8071
1,2-Dimethoxyethane
용매

반응 조건

온도
-5 °C

실험 절차

N-Chlorosuccinimide (50 mg, 0.37 mmol) was added slowly with stirring to a precooled (−5° C.) suspension, prepared by mixing a solution of 20 (75 mg, 0.31 mmol) in 1,2-dimethoxyethane (25 ml) with a solution of sodium azide (81 mg, 1.24 mmol) in water (0.23 ml). The reaction mixture was allowed to proceed for 2 h at 0° C. with stirring and the solvent was removed in vacuo. The resulting residue was purified by silica gel column chromatography using chloroform:methanol (90:10, v/v) as eluent to afford 21b (46 mg, 47%) as a viscous oil.

후처리

  1. customprepared
  2. stirringwith stirring
  3. customthe solvent was removed in vacuo
  4. customThe resulting residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-3a5e5be6bbd44d73bed28cafe5fbe21a
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589077B2

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