Ammonia → HCID 15168483, compound

HRID 484428Notes

Reaction equation

HRID 484428 reaction equation
Cl[C:2]([C:4]1[C:13]2[C:8](=[CH:9][C:10]([Cl:15])=[CH:11][C:12]=2[Cl:14])[N:7]=[C:6]([C:16]([O:18][CH3:19])=[O:17])[CH:5]=1)=[O:3].[NH3:20]>O1CCCC1>[NH2:20][C:2]([C@@H:4]1[C:13]2[C:8](=[CH:9][C:10]([Cl:15])=[CH:11][C:12]=2[Cl:14])[NH:7][C@@H:6]([C:16]([O:18][CH3:19])=[O:17])[CH2:5]1)=[O:3]

Participants

4

Reactant 2

HCID 222AmmoniaHCID 15168481HCID 15168481, compound

Product 1

HCID 15168483HCID 15168483, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

4-Chlorocarbonyl-5,7-dichloro-2-methoxycarbonylquinoline (1.5 g) was dissolved in dry tetrahydrofuran (20 ml) at 0° C. and an ice-cool solution of tetrahydrofuran (150 ml), presaturated with ammonia gas, was added in one portion. After stirring at room temperature for 30 minutes the white solid which precipitated was collected by filtration and dried (1.4 g). A portion of this solid (1 g) was suspended in glacial acetic acid (20 ml) and sodium cyanoborohydride (1.3 g) was added in portions. When the addition was complete the reaction mixture was heated at 50° C. for 2 h, cooled and stirred at room temperature for 14 h. The solution was diluted with dichloromethane (to a volume of 100 ml) and ice cold 50% sodium hydroxide solution added cautiously until a pH of 14 was attained. The organic layer was separated and the aqueous layer was re-extracted with dichloromethane (2×100 ml). The combined organic fractions were washed with brine (1×150 ml), dried (Na2SO4), filtered and concentrated in vacuo to give a residue which was purified by chromatrography on silica gel with 2% methanol in dichloromethane as eluent to give, as the less polar isomer, trans-4-aminocarbonyl-5,7-dichloro-2-methoxycarbonyl-1,2,3,4-tetrahydroquinoline (0.15 g, m.p. 217°- 229° C. [recrystallised from methanol]); δ (360 MHz, DMSO) 1.83 (1H, m, CHACHBHCCHD), 2.32 (1H, dm, J=13.2 Hz, CHACHBHCCHD), 3.72 (3H, s, CH3), 3.78 (1H, dd, J=5.8 and 2.0 Hz, CHACHBHCCHD), 4.01 (1H, dd, J=12.2 and 2.1 Hz, CHACHBHCCHD), 6.63 (1H, d, J=2.1 Hz, 6-H or 8-H), 6.66 (1H, br, s, NH), 6.78 (1H, d, J=2.1 Hz, 6-H or 8-H), 7.02 (1H, br, s, NH), 7.51 (1H, br, s, NH); m/e 302 (M+), 198 (100%, M-H, CONH2 and CO2CH 3); Found: C, 47.46; H, 3.95; N, 9.18 C12H12Cl2N2O3 requires C, 47.55; H, 3.99; N, 9.24%; and as the more polar isomer, cis-4-aminocarbonyl-5,7-dichloro-2-methoxycarbonyl-1,2,3,4-tetrahydroquinoline (0.14 g, m.p. 203°-204° C.); δ (360 MHz, DMSO), 2.05 (1H, m, CHACHBHCCHD), 2.52 (1H, m, CHACHBHCCHD), 3.54 (3H, s, CH3), 3.71 (1H, dd, J=7.2 and 3.4 Hz, CHACHBHCCHD), 4.11 (1H, dd, J=5.2 and 3.2 Hz, CHACHBHCCHD), 6.61 (1H, d, J=2.1 Hz, 6-H or 8-H), 6.70 (1H, d, J=2.1 Hz, 6-H or 8-H), 6.84 (2H, br, s, CONH2), 7.20 (1H, br, s, NH); m/e (CI+) 303 (M+1); Found: C, 47.38; H, 3.98; N, 9.14. C12H12Cl2N2O3 requires C, 47.55; H, 3.99; N, 9.24%.

Workup

  1. additionwas added in one portion
  2. customprecipitated
  3. filtrationwas collected by filtration
  4. customdried (1.4 g)
  5. additionsodium cyanoborohydride (1.3 g) was added in portions
  6. additionWhen the addition
  7. temperaturewas heated at 50° C. for 2 h
  8. temperaturecooled
  9. stirringstirred at room temperature for 14 h
  10. additionThe solution was diluted with dichloromethane (to a volume of 100 ml) and ice cold 50% sodium hydroxide solution
  11. additionadded cautiously until a pH of 14
  12. customThe organic layer was separated
  13. extractionthe aqueous layer was re-extracted with dichloromethane (2×100 ml)
  14. washThe combined organic fractions were washed with brine (1×150 ml)
  15. dry with materialdried (Na2SO4)
  16. filtrationfiltered
  17. concentrationconcentrated in vacuo
  18. customto give a residue which
  19. customwas purified by chromatrography on silica gel with 2% methanol in dichloromethane as eluent

Sources & evidence

ORD record
ord-6ec1bcfac8c04c148ca0e8788c25686f
Source dataset
uspto-grants-1993_07
Patent number
US05231102

Reaction notes

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