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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 178494681, 화합물 → HCID 178424690, 화합물

HRID 1488114
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인쇄 미리보기

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HRID 1488114 반응식
[Cl:1][C:2]1[N:3]=[C:4]([CH2:19][O:20]C)[NH:5][C:6]=1[C:7]1[C:8]([CH3:18])=[CH:9][C:10]([CH3:17])=[C:11]([CH:16]=1)[C:12]([O:14]C)=[O:13]>Br>[Cl:1][C:2]1[N:3]=[C:4]([CH2:19][OH:20])[NH:5][C:6]=1[C:7]1[C:8]([CH3:18])=[CH:9][C:10]([CH3:17])=[C:11]([CH:16]=1)[C:12]([OH:14])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178494681HCID 178494681, 화합물2회

생성물 1

HCID 178424690HCID 178424690, 화합물수율 59.4%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

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온도
90 °C

실험 절차

Into a 50-mL round-bottom flask, was placed a solution of methyl 5-(4-chloro-2-(methoxymethyl)-1H-imidazol-5-yl)-2,4-dimethylbenzoate (compound 230.5, 20 mg, 0.06 mmol) in HBr (5 mL, 40% in AcOH). The reaction mixture was stirred overnight at 90° C. The resulting mixture was concentrated under reduced pressure. This resulted in 10 mg (55%) of the title compound as a yellow crude solid.

후처리

  1. customInto a 50-mL round-bottom flask, was placed
  2. concentrationThe resulting mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-a5a41ad08db44c28b87b83c900cf2d5a
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428502B2

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