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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → 4-((8-((5-Cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)carbamoyl)-2-formyl-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)methyl)-1-methyl-3-oxopiperazine 1-oxide

HRID 1778109
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HRID 1778109 반응식
ClC1C=C(C=CC=1)C(OO)=[O:6].[C:12]([C:14]1[C:15]([NH:44][CH2:45][CH2:46][O:47][CH3:48])=[CH:16][C:17]([NH:20][C:21]([N:23]2[C:32]3[C:27](=[CH:28][C:29]([CH2:35][N:36]4[CH2:41][CH2:40][N:39]([CH3:42])[CH2:38][C:37]4=[O:43])=[C:30]([CH:33]=[O:34])[N:31]=3)[CH2:26][CH2:25][CH2:24]2)=[O:22])=[N:18][CH:19]=1)#[N:13]>C(Cl)(Cl)Cl.C(Cl)Cl>[C:12]([C:14]1[C:15]([NH:44][CH2:45][CH2:46][O:47][CH3:48])=[CH:16][C:17]([NH:20][C:21]([N:23]2[C:32]3[N:31]=[C:30]([CH:33]=[O:34])[C:29]([CH2:35][N:36]4[CH2:41][CH2:40][N+:39]([O-:6])([CH3:42])[CH2:38][C:37]4=[O:43])=[CH:28][C:27]=3[CH2:26][CH2:25][CH2:24]2)=[O:22])=[N:18][CH:19]=1)#[N:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 118036971Roblitinib

생성물 1

HCID 1180368704-((8-((5-Cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)carbamoyl)-2-formyl-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)methyl)-1-methyl-3-oxopiperazine 1-oxide

시약·촉매·용매 2

HCID 6212Chloroform용매HCID 6344Dichloromethane용매

실험 절차

3-Chlorobenzoperoxoic acid (9.3 mg, 0.041 mmol) was added to a solution of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide (Example 83, 20 mg, 0.039 mmol) in CHCl3 (0.1 ml) at 0° C. After stirring for 20 min, the mixture was warmed to room temperature and stirred for another 2 h. The reaction mixture was diluted with DCM and washed with sat. aq. NaHCO3. The aqueous layer was back-extracted with DCM (2×). The combined organic layers were dried over Na2SO4 and evaporated. The residue was triturated with Et2O to give the title compound as a light purple solid.

후처리

  1. stirringstirred for another 2 h
  2. washwashed with sat. aq. NaHCO3
  3. extractionThe aqueous layer was back-extracted with DCM (2×)
  4. dry with materialThe combined organic layers were dried over Na2SO4
  5. customevaporated
  6. customThe residue was triturated with Et2O

출처 및 근거

ORD 기록
ord-5e25276cfa3d4100aa6936e3963840e3
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266883B2

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