Hydrochloric Acid → HCID 10006005, compound

HRID 1367098Notes

Reaction equation

HRID 1367098 reaction equation
C[O:2][C:3](=[O:36])[CH2:4][CH:5]([C:22]1[CH:27]=[CH:26][C:25]([O:28][CH:29]([F:31])[F:30])=[C:24]([O:32][CH:33]([F:35])[F:34])[CH:23]=1)[N:6]1[CH2:14][C:13]2[C:8](=[C:9]([NH:15][C:16]([CH:18]3[CH2:20][CH2:19]3)=[O:17])[CH:10]=[CH:11][CH:12]=2)[C:7]1=[O:21].[OH-].[Na+].Cl>O1CCCC1.O>[F:35][CH:33]([F:34])[O:32][C:24]1[CH:23]=[C:22]([CH:5]([N:6]2[CH2:14][C:13]3[C:8](=[C:9]([NH:15][C:16]([CH:18]4[CH2:20][CH2:19]4)=[O:17])[CH:10]=[CH:11][CH:12]=3)[C:7]2=[O:21])[CH2:4][C:3]([OH:36])=[O:2])[CH:27]=[CH:26][C:25]=1[O:28][CH:29]([F:31])[F:30]

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 66920336HCID 66920336, compound

Product 1

HCID 10006005HCID 10006005, compoundYield 70.5%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 3-(3,4-bis-difluoromethoxy-phenyl)-3-[7-(cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-propionic acid methyl ester (2.0 g, 4 mmol) in tetrahydrofurane (20 ml) was added NaOH (0.8 ml of 10 N) at room temperature. The solution was stirred overnight at room temperature. The resulted suspension was filtered to get a white solid. The solid was dissolved in water (30 ml) and added conc. HCl dropwise until the pH is about 4. The resulted mixture was extracted with CH2Cl2 (3×40 ml). The organic layer was dried over Na2SO4, filtered and concentrated to give 3-(3,4-bis-difluoromethoxy-phenyl)-3-[7-(cyclopropanecarbonyl-amino)-1-oxo-1,3-dihydro-isoindol-2-yl]-propionic acid as a white solid (1.4 g, 70%): mp, 94-96° C.; 1H NMR (CDCl3) δ 0.86-0.93 (m, 2H, cyclopropyl ring CH2), 1.06-1.12 (m, 2H, cyclopropyl ring CH2), 1.65-1.71 (m, 1H, cyclopropyl ring CH, 3.13 (dd, J=6, 16 Hz, 1H, CHHCO), 3.32 (dd, J=9, 16 Hz, 1H, CHHCO), 4.15 (d, J=15 Hz, 1H, CHHN), 4.36 (d, J=15 Hz, 1H, CHHN), 5.78-5.84 (m, 1H, CHN), 6.21 (t, JH-F=75 Hz, 1H, OCF2H), 6.24 (t, JH-F=75 Hz, 1H, OCF2H), 7.01 (d, J=7.5 Hz, 1H, Ar), 7.26-7.28 (m, 3H, Ar), 7.44 (t, J=7.5 Hz, 1H, Ar), 8.43 (d, J=7.5 Hz, 1H, Ar), 10.42 (s, 1H, NHCO); 13C NMR (CDCl3): 8.35, 8.38, 16.14, 36.55, 47.00, 51.29, 99.24, 111.36, 111.42, 115.60, 116.84, 117.02, 118.03, 119.74, 119.79, 121.59, 122.76, 125.46, 133.61, 137.09, 138.03, 141.12, 142.21, 142.38, 142.43, 169.63, 173.03, 173.82. Anal. Calcd. for C23H20F4N2O6: C, 55.65; H, 4.06; N, 5.64. Found: C, 55.33; H, 3.96; N, 5.38.

Workup

  1. filtrationThe resulted suspension was filtered
  2. customto get a white solid
  3. extractionThe resulted mixture was extracted with CH2Cl2 (3×40 ml)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-c08e91a820464f70b4e7a92745cb22ec
Source dataset
uspto-grants-2011_02
Patent number
US07893102B2

Reaction notes

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