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Dimethylformamide → Ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-2-(2-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)-2-oxoethyl)-3-oxopentanoate

HRID 1056234
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1056234
[CH2:1]([O:8][CH2:9][C@@H:10]([NH:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[C:11](=[O:18])[CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].Br[CH2:34][C:35]([C:37]1[CH:46]=[CH:45][CH:44]=[C:43]2[C:38]=1[N:39]=[C:40]([NH:48][C:49]1([CH3:52])[CH2:51][CH2:50]1)[C:41]([CH3:47])=[N:42]2)=[O:36].CN(C=O)C>[NH4+].[Cl-]>[CH2:1]([O:8][CH2:9][CH:10]([NH:19][C:20]([O:22][C:23]([CH3:25])([CH3:24])[CH3:26])=[O:21])[C:11](=[O:18])[CH:12]([CH2:34][C:35]([C:37]1[CH:46]=[CH:45][CH:44]=[C:43]2[C:38]=1[N:39]=[C:40]([NH:48][C:49]1([CH3:52])[CH2:51][CH2:50]1)[C:41]([CH3:47])=[N:42]2)=[O:36])[C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 897821052-Bromo-1-(2-methyl-3-((1-methylcyclopropyl)amino)-5-quinoxalinyl)ethanoneHCID 131736415(R)-ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-3-oxopentanoate

Produkt 1

HCID 89781948
Ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-2-(2-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)-2-oxoethyl)-3-oxopentanoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 25517Ammonium ChlorideLösungsmittel

Versuchsvorschrift

To a 50-mL round-bottomed flask was added (R)-ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-3-oxopentanoate (612) (0.51 g, 1.19 mmol), K2CO3 (0.41 g, 2.97 mmol), 2-bromo-1-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)ethanone (611) (0.63 g, 1.90 mmol), and DMF (4 mL). The reaction mixture was stirred at RT for 1 h. The reaction mixture was diluted with sat NH4Cl (5 mL) and extracted with EtOAc (10 mL). The organic extract was washed with water (5 mL), dried over Na2SO4, and concentrated. Ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-2-(2-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)-2-oxoethyl)-3-oxopentanoate (355a) was obtained as a light yellow oil and used without further purification. m/z (ESI, +ve) 619.3 (M+H)+. To a 15-mL glass tube was added ethyl 5-(benzyloxy)-4-((tert-butoxycarbonyl)amino)-2-(2-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)-2-oxoethyl)-3-oxopentanoate (355a), crude from previous step, NH4OAc (0.37 g, 4.75 mmol), EtOH (5 mL), and AcOH (1.5 mL). The tube was sealed and heated at 45° C. for 16 h. The reaction mixture was cooled to RT and was concentrated to half of its volume. The mixture was diluted with EtOAc (10 mL) and water (5 mL). The organic extract was washed with NaOH (1 N, 5 mL), water (5 mL), brine (5 mL), dried over Na2SO4, and concentrated. The crude material was absorbed onto a plug of silica gel and purified by chromatography through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 10-30% EtOAc in hexanes to give ethyl 2-(2-(benzyloxy)-1-((tert-butoxycarbonyl)amino)ethyl)-5-(2-methyl-3-((1-methylcyclopropyl)amino)quinoxalin-5-yl)-1H-pyrrole-3-carboxylate (355b) (0.28 g, 40% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 11.75 (br. s., 1H), 8.06 (d, J=1.96 Hz, 1H), 7.92 (dd, J=1.17, 7.63 Hz, 1H), 7.62 (dd, J=1.17, 8.02 Hz, 1H), 7.49 (s, 1H), 7.39 (t, J=7.82 Hz, 1H), 7.24-7.31 (m, 5H), 7.12 (br. d, J=9.20 Hz, 1H), 5.61-5.72 (m, 1H), 4.44-4.58 (m, 2H), 4.23 (q, J=7.04 Hz, 2H), 3.62-3.67 (m, 2H), 2.49 (s, 3H), 1.58 (s, 3H), 1.41 (s, 9H), 1.29 (t, J=7.04 Hz, 3H), 0.97-1.02 (m, 2H), 0.84-0.89 (m, 2H). m/z (ESI, +ve) 600.2 (M+H)+.

Aufarbeitung

  1. extractionextracted with EtOAc (10 mL)
  2. extractionThe organic extract
  3. washwas washed with water (5 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-2310cfda00b44e8fbcfbd69fc779a903
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09394297B2

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