Sodium Bicarbonate → N-cyclohexyl-N-(2-(2-(5-hydroxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-8-yl)ethylamino)ethyl)-3-(3-(1-methyl-1H-pyrazol-4-yl)phenethoxy)propanamide

HRID 909888Notes

Reaction equation

HRID 909888 reaction equation
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH:13]1([N:19]([CH2:39][CH:40](OC)OC)[C:20](=[O:38])[CH2:21][CH2:22][O:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([C:32]3[CH:33]=[N:34][N:35]([CH3:37])[CH:36]=3)[CH:27]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.Cl.[NH2:46][CH2:47][CH2:48][C:49]1[C:54]2[O:55][CH2:56][C:57](=[O:59])[NH:58][C:53]=2[C:52]([OH:60])=[CH:51][CH:50]=1.C(=O)(O)[O-].[Na+].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>O1CCCC1.C(O)(=O)C.CN1C(=O)CCC1.O>[CH:13]1([N:19]([CH2:39][CH2:40][NH:46][CH2:47][CH2:48][C:49]2[C:54]3[O:55][CH2:56][C:57](=[O:59])[NH:58][C:53]=3[C:52]([OH:60])=[CH:51][CH:50]=2)[C:20](=[O:38])[CH2:21][CH2:22][O:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([C:32]3[CH:33]=[N:34][N:35]([CH3:37])[CH:36]=3)[CH:27]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

10

Reactant 5

HCID 516892Sodium Bicarbonate2×HCID 521998p-Toluenesulfonic acid monohydrateHCID 5049666Sodium triacetoxyborohydrideHCID 59290438N-Cyclohexyl-N-(2,2-dimethoxyethyl)-3-(3-(1-methyl-1H-pyrazol-4-yl)phenethoxy)propanamideHCID 669633558-(2-Aminoethyl)-5-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one hydrochloride

Product 1

HCID 53245747N-cyclohexyl-N-(2-(2-(5-hydroxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-8-yl)ethylamino)ethyl)-3-(3-(1-methyl-1H-pyrazol-4-yl)phenethoxy)propanamideYield 52.3%

Reagents, catalysts & solvents 4

HCID 176Acetic AcidSolventHCID 962WaterSolventHCID 8028TetrahydrofuranSolventHCID 13387N-methyl-2-pyrrolidoneSolvent

Conditions

Temperature
20 °C

Procedure

p-Toluenesulfonic acid monohydrate (5.31 g) was added in one portion to N-cyclohexyl-N-(2,2-dimethoxyethyl)-3-(3-(1-methyl-1H-pyrazol-4-yl)phenethoxy)propanamide (7.74 g, prepared as in Example 2a, Step ii)) in tetrahydrofuran (60 mL). The resulting solution was stirred at 20° C. for 30 min. This solution was added to a stirred mixture of 8-(2-aminoethyl)-5-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one hydrochloride (4.27 g), sodium bicarbonate (4.40 g), water (6 mL) and NMP (60 mL). The mixture was stirred for 10 min. and sodium triacetoxyborohydride (9.25 g) and acetic acid (1 mL) were added. The mixture was stirred for 3 h. The reaction mixture was neutralised with saturated sodium hydrogen carbonate (100 mL) and extracted into ethyl actate (5×100 mL). Methanol (50 mL) was added and the organic was washed with a 1:1 mixture of water and saturated brine (2×70 mL). The organic was dried over magnesium sulfate, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 50 to 100% isohexane in ethyl acetate, then elution gradient 2 to 10% methanol in dichloromethane to afford N-cyclohexyl-N-(2-(2-(5-hydroxy-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-8-yl)ethylamino)ethyl)-3-(3-(1-methyl-1H-pyrazol-4-yl)phenethoxy)propanamide (5.38 g) as a gum.

Workup

  1. stirringThe mixture was stirred for 10 min.
  2. stirringThe mixture was stirred for 3 h
  3. extractionextracted into ethyl actate (5×100 mL)
  4. additionMethanol (50 mL) was added
  5. washthe organic was washed with a 1:1 mixture of water and saturated brine (2×70 mL)
  6. dry with materialThe organic was dried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customto afford crude product
  10. customThe crude product was purified by flash silica chromatography, elution gradient 50 to 100% isohexane in ethyl acetate
  11. washelution gradient 2 to 10% methanol in dichloromethane

Sources & evidence

ORD record
ord-dbab2c0a55b44d2bb341915ebf196777
Source dataset
uspto-grants-2011_09
Patent number
US08017602B2

Reaction notes

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