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O-Phenylenediamine → HCID 16006048, 화합물

HRID 1694835
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HRID 1694835 반응식
[NH:1]([C:8](=[O:28])[CH:9]([C:19]1[CH:27]=[CH:26][C:22]([C:23]([OH:25])=O)=[CH:21][N:20]=1)[C:10]([NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCN=C=NCCCN(C)C.[CH:40]1[CH:41]=[CH:42][C:43]2[N:48](O)N=[N:46][C:44]=2[CH:45]=1.C1(N)C=CC=CC=1N>CN(C=O)C>[NH2:46][C:44]1[CH:45]=[CH:40][CH:41]=[CH:42][C:43]=1[NH:48][C:23]([C:22]1[CH:26]=[CH:27][C:19]([CH:9]([C:8]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[O:28])[C:10]([NH:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:11])=[N:20][CH:21]=1)=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7243O-PhenylenediamineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 59376457HCID 59376457, 화합물

생성물 1

HCID 16006048HCID 16006048, 화합물수율 37%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

To a solution of 6-[2-anilino-1-(anilinocarbonyl)-2-oxoethyl]nicotinic acid (35 mg, 0.093 mmol) in DMF (1 mL) at room temperature was added EDCI (22 mg, 0.11 mmol) and HOBT (14 mg, 0.10 mmol). The solution was stirred for 30 min and 1,2-phenylenediamine (34 mg, 0.31 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 18 h and purified by reverse phase HPLC (5% to 80% MeCN in water) to give 2-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-N,N′-diphenylmalonamide (16 mg, TFA salt, 21% from methyl 6-[2-anilino-1-(anilinocarbonyl)-2-oxoethyl]nicotinate) as a white solid: ESIMS calcd 466.2 (M++H), found 466.1 (M++H).

후처리

  1. stirringThe reaction mixture was stirred at room temperature for 18 h
  2. custompurified by reverse phase HPLC (5% to 80% MeCN in water)

출처 및 근거

ORD 기록
ord-a363bd758a294a7b946a3d1065fd3643
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158825B2

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