Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 8-[3-(Trifluoromethyl)-8-quinolinyl]-1,4-dioxa-8-azaspiro[4.5]decane | HCID 59204865 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59204871 | HCID 59204871 | 66.6% |
Reaction Steps
A solution of 8-(1.4-dioxa-8-azaspiro[4.5]dec-8-yl)-3-(trifluoromethyl)quinoline (Step 3, 0.19 g) in tetrahydrofuran (3 mL) was treated with 2N aqueous HCl (1 mL) and then stirred at 40° C. for 18 hours. The mixture was cooled to room temperature and concentrated on a rotary evaporator. The residue was taken up in CH2Cl2, washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated on a rotary evaporator to give 0.11 g of the desired product as a yellow oil; MS (ES) m/z (relative intensity); 295 (M+H)+ (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671056B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-b380d390cd954acc847f9a7a7086bd42 |
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| Source note | uspto-grants-2010_03 |
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