Hydrochloric Acid → Ethyl 2-amino-2-methyl-4-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)butanoate

HRID 1506505Notes

Reaction equation

HRID 1506505 reaction equation
C1(C(=[N:14][C:15]([CH3:51])([CH2:21][CH2:22][C:23]2[CH:24]=[C:25]3[C:48](=[CH:49][CH:50]=2)[C:29]2=[N:30][O:31][C:32]([C:33]4[C:37]([C:38]([F:41])([F:40])[F:39])=[C:36]([C:42]5[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=5)[O:35][N:34]=4)=[C:28]2[CH2:27][CH2:26]3)[C:16]([O:18][CH2:19][CH3:20])=[O:17])C2C=CC=CC=2)C=CC=CC=1.Cl.C(=O)([O-])[O-].[K+].[K+]>C(OCC)C>[NH2:14][C:15]([CH3:51])([CH2:21][CH2:22][C:23]1[CH:24]=[C:25]2[C:48](=[CH:49][CH:50]=1)[C:29]1=[N:30][O:31][C:32]([C:33]3[C:37]([C:38]([F:39])([F:40])[F:41])=[C:36]([C:42]4[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=4)[O:35][N:34]=3)=[C:28]1[CH2:27][CH2:26]2)[C:16]([O:18][CH2:19][CH3:20])=[O:17]

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 86669932Ethyl 2-(diphenylmethyleneamino)-2-methyl-4-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)butanoate

Product 1

HCID 67170372Ethyl 2-amino-2-methyl-4-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)butanoate

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

To a stirred solution of ethyl 2-(diphenylmethyleneamino)-2-methyl-4-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)butanoate (Preparation 93A, 36 mg, 0.052 mmol) in diethyl ether (3 mL) was added 4 M aqueous solution of HCl (120 μL, 0.480 mmol). The mixture was stirred at room temperature for 30 min. The ether layer was separated and extracted with water (1 mL). The aqueous extract was combined with the aqueous layer in the reaction. The mixture was basified with solid potassium carbonate and extracted with ethyl acetate (4×1.5 ml). The combined ethyl acetate extracts were dried (sodium sulfate) and concentrated under reduced pressure to give a glassy solid. The individual enantiomers were separated using a Lux-Cellulose-2 column under SFC conditions (20% IPA with 0.1% EA in CO2). Isomer 1 (Preparation 94A, 8 mg), retention time on chiral HPLC, 8.3 min; Isomer 2 (Preparation 94A, 6 mg), retention time on chiral HPLC, 9.3 min. The absolute stereochemistry at the carbon anchoring the secondary alcohol, of Isomer 1 and Isomer 2, was not determined.

Workup

  1. customThe ether layer was separated
  2. extractionextracted with water (1 mL)
  3. extractionThe aqueous extract
  4. customwas combined with the aqueous layer in the reaction
  5. extractionextracted with ethyl acetate (4×1.5 ml)
  6. dry with materialThe combined ethyl acetate extracts were dried (sodium sulfate)
  7. concentrationconcentrated under reduced pressure
  8. customto give a glassy solid
  9. customThe individual enantiomers were separated
  10. customIsomer 1 (Preparation 94A, 8 mg), retention time on chiral HPLC, 8.3 min

Sources & evidence

ORD record
ord-c94700694bcf461b806b5e9112b96da0
Source dataset
uspto-grants-2015_12
Patent number
US09216972B2

Reaction notes

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