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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 11189100, 화합물 → HCID 11163028, 화합물

HRID 2053420
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인쇄 미리보기

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HRID 2053420 반응식
C([N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[C:13]1[C:14](=[O:30])[NH:15][C:16]2[C:21]([C:22]=1[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[CH:20][C:19]([Cl:29])=[CH:18][CH:17]=2)C1C=CC=CC=1>ClC(OC(Cl)=O)C>[Cl:29][C:19]1[CH:20]=[C:21]2[C:16](=[CH:17][CH:18]=1)[NH:15][C:14](=[O:30])[C:13]([C:9]1[NH:10][CH:11]=[CH:12][N:8]=1)=[C:22]2[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 11189100HCID 11189100, 화합물

생성물 1

HCID 11163028HCID 11163028, 화합물수율 66%

시약·촉매·용매 1

HCID 5213051-Chloroethyl chloroformate용매

반응 조건

온도
100 °C

실험 절차

A solution of 3-(1-benzyl-1H-imidazol-2-yl)-6-chloro-4-phenyl-1H-quinolin-2-one (110 mg) in α-chloroethylchloroformate (5 mL) was heated at 100° C. for 2 hr. The reaction was evaporated and the resulting residue was dried in vacuo. The residue was dissolved in HOAc (5 mL) and NH4Ac (100 mg) was added. The reaction mixture was heated at 100° C. for 12 hr. Solvents were removed and the title compound was isolated by reversed phase HPLC. Yield 66%.

후처리

  1. customThe reaction was evaporated
  2. customthe resulting residue was dried in vacuo
  3. dissolutionThe residue was dissolved in HOAc (5 mL)
  4. additionNH4Ac (100 mg) was added
  5. customSolvents were removed

출처 및 근거

ORD 기록
ord-5d538ca4b9a049c6a8bc36d28474916d
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326788B2

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