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Dimethylformamide → n-(2-Amino-4-fluorophenyl)-6-(4-(2-(((5-fluoro-2-oxoindolin-3-ylidene)-hydrazono)methyl)-3,5-dimethyl-1h-pyrrole-4-carboxamido)butylamino)nicotinamide

HRID 1695047
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HRID 1695047 반응식
[F:1][C:2]1[CH:3]=[C:4]2C(=[CH:9][CH:10]=1)NC(=O)[C:5]2=[N:12][N:13]=CC1(C)CC(C)(C(O)=O)CN1.Cl.C(N=C=NCCCN(C)C)C.[OH:37][C:38]1C2N=NNC=2[CH:41]=[CH:40][CH:39]=1.C([N:49]([CH2:52][CH3:53])[CH2:50][CH3:51])C.[NH2:54][C:55]1[CH:60]=[C:59]([F:61])[CH:58]=[CH:57][C:56]=1[NH:62][C:63](=[O:76])[C:64]1[CH:69]=[CH:68][C:67]([NH:70][CH2:71][CH2:72][CH2:73][CH2:74][NH2:75])=[N:66][CH:65]=1.[CH3:77][N:78]([CH:80]=[O:81])C>[Cl-].[Na+].O>[NH2:54][C:55]1[CH:60]=[C:59]([F:61])[CH:58]=[CH:57][C:56]=1[NH:62][C:63](=[O:76])[C:64]1[CH:69]=[CH:68][C:67]([NH:70][CH2:71][CH2:72][CH2:73][CH2:74][NH:75][C:38]([C:39]2[C:40]([CH3:41])=[C:52]([CH:53]=[N:13][N:12]=[C:5]3[C:4]4[C:77](=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=4)[NH:78][C:80]3=[O:81])[NH:49][C:50]=2[CH3:51])=[O:37])=[N:66][CH:65]=1
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참가 물질

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반응물 6

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 57993725N-(2-amino-4-fluorophenyl)-6-(4-aminobutylamino)nicotinamideHCID 1372525122-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-4-carboxylic acidHCID 178418300HCID 178418300, 화합물

생성물 1

HCID 136492168n-(2-Amino-4-fluorophenyl)-6-(4-(2-(((5-fluoro-2-oxoindolin-3-ylidene)-hydrazono)methyl)-3,5-dimethyl-1h-pyrrole-4-carboxamido)butylamino)nicotinamide수율 69%

시약·촉매·용매 1

HCID 57417360Sodium chloride; water용매

실험 절차

2-(((5-Fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-4-carboxylic acid (328 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (384 mg, 2 mmol), hydroxybenzotriazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and N-(2-amino-4-fluorophenyl)-6-(4-aminobutylamino)nicotinamide (333 mg, 1.05 mmol) were added. The mixture was stirred for 20 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (433 mg, 69%) as a red solid. 1H NMR (DMSO-d6)δ1.58 (m, 4H, CH2CH2), 2.32 (s, 3H, pyrrole-CH3), 2.42 (s, 3H, pyrrole-CH3), 3.24 (m, 2H, CH2), 3.35 (m, 2H, CH2), 5.18 (s, 2H, benzene-NH2), 6.33 (m, 1H), 6.50 (m, 2H), 6.85 (m, 1H), 7.06 (m, 1H), 7.20 (m, 2H), 7.67 (s, 1H), 7.89 (d, J=8.0 Hz, 1H), 8.33 (d, J=8.0 Hz, 1H), 8.63 (s, 2H), 9.29 (s, 1H, benzene-NH), 10.74 (s, 1H, indolinone-NH), 11.83 (s, 1H, pyrrole-NH). LC-MS (m/z) 628 (M+1).

후처리

  1. additionwere added
  2. filtrationThe solids were collected by vacuum filtration
  3. washwashed with water
  4. customdried under vacuum

출처 및 근거

ORD 기록
ord-cfb35397a3004eb2817f1ab092101db8
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158656B2

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