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Chlorosuccinimide → HCID 178494681, 화합물

HRID 1488113
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HRID 1488113 반응식
[CH3:1][O:2][CH2:3][C:4]1[NH:5][C:6]([C:9]2[C:10]([CH3:20])=[CH:11][C:12]([CH3:19])=[C:13]([CH:18]=2)[C:14]([O:16][CH3:17])=[O:15])=[CH:7][N:8]=1.C1C(=O)N([Cl:28])C(=O)C1>C(Cl)(Cl)Cl>[Cl:28][C:7]1[N:8]=[C:4]([CH2:3][O:2][CH3:1])[NH:5][C:6]=1[C:9]1[C:10]([CH3:20])=[CH:11][C:12]([CH3:19])=[C:13]([CH:18]=1)[C:14]([O:16][CH3:17])=[O:15]
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참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 90033625Methyl 5-(2-(methoxymethyl)-1H-imidazol-5-yl)-2,4-dimethylbenzoate2회

생성물 1

HCID 178494681HCID 178494681, 화합물수율 38%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

Into a 100-mL round-bottom flask, was placed a solution of methyl 5-(2-(methoxymethyl)-1H-imidazol-5-yl)-2,4-dimethylbenzoate (compound 230.5, 70 mg, 0.26 mmol) in chloroform (6 mL). NCS (35 mg, 0.26 mmol) was added to the reaction. The reaction mixture was stirred overnight at room temperature, then quenched with 1 mL of water. The aqueous phase was extracted with 2×5 mL of dichloromethane and the combined organic layers were concentrated under reduced pressure. The residue was applied onto a silica gel chromatography with ethyl acetate/petroleum ether (1:10) as eluent to yield 30 mg (38%) of the title compound as a white crude solid.

후처리

  1. customInto a 100-mL round-bottom flask, was placed
  2. customquenched with 1 mL of water
  3. extractionThe aqueous phase was extracted with 2×5 mL of dichloromethane
  4. concentrationthe combined organic layers were concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f4e0c7368fda432583ebebe69f4f668b
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428502B2

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