Hydrochloric Acid → N-((6-(aminomethyl)-4-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamide

HRID 1476971Notes

Reaction equation

HRID 1476971 reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[C:13]([CH3:15])[C:12]([CH2:16][NH:17][C:18]([C:20]2[C:21]3[C:22]([CH3:33])=[CH:23][N:24]([CH:30]([CH3:32])[CH3:31])[C:25]=3[CH:26]=[C:27]([Br:29])[CH:28]=2)=[O:19])=[C:11]([O:34]C)[N:10]=1)(C)(C)C.Cl>O1CCCC1>[NH2:7][CH2:8][C:9]1[NH:10][C:11](=[O:34])[C:12]([CH2:16][NH:17][C:18]([C:20]2[C:21]3[C:22]([CH3:33])=[CH:23][N:24]([CH:30]([CH3:31])[CH3:32])[C:25]=3[CH:26]=[C:27]([Br:29])[CH:28]=2)=[O:19])=[C:13]([CH3:15])[CH:14]=1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 68210118tert-butyl((5-((6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamido)methyl)-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate

Product 1

HCID 67467538N-((6-(aminomethyl)-4-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamideYield 82.3%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
80 °C

Procedure

To a stirred solution of tert-butyl((5-((6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamido)methyl)-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate (500 mg, 0.894 mmol) in Tetrahydrofuran (THF) (5 mL) was added 6N HCl (15 mL, 15.00 mmol). The reaction was stirred under N2 with heating at 80° C. for 18 hr. The reaction was cooled to RT and evaporated to dryness under vacuum. The remaining was purified by silica gel chromatography (Analogix, SF25-40 g, 0 to 10% (5% NH4OH in MeOH) in CH2C12). The pure fractions were combined and evaporated to dryness under vacuum. Dissolved with a small volume of CH2C12, scratched out by slowly adding hexanes, filtered, washed with hexanes and dried under vacuum to give the product N-((6-(aminomethyl)-4-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxamide (328 mg, 0.736 mmol, 82% yield) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ=8.26 (t, J=5.1 Hz, 1H), 7.76 (d, J=1.8 Hz, 1H), 7.33 (d, J=1.0 Hz, 1H), 7.01 (d, J=1.5 Hz, 1H), 6.01 (s, 1H), 5.77 (s, 0H), 4.74 (quin, J=6.6 Hz, 1H), 4.32 (d, J=5.1 Hz, 2H), 3.46 (s, 2H), 2.25 (s, 3H), 2.14 (s, 3H), 1.39 (d, J=6.8 Hz, 6H). MS(ES)+m/e 445.2 [M+H]+.

Workup

  1. temperatureThe reaction was cooled to RT
  2. customevaporated to dryness under vacuum
  3. customThe remaining was purified by silica gel chromatography (Analogix
  4. customevaporated to dryness under vacuum
  5. dissolutionDissolved with a small volume of CH2C12
  6. filtrationfiltered
  7. washwashed with hexanes
  8. customdried under vacuum

Sources & evidence

ORD record
ord-568982bd02b64788b53b1b49e576680a
Source dataset
uspto-grants-2016_08
Patent number
US09402836B2

Reaction notes

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