Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 22220329 | HCID 22220329 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178420598 | HCID 178420598 | 80.1% |
Reaction Steps
A mixture of 4-(1,4-dioxa-8-azaspiro(4.5)dec-8-yl)benzonitrile benzaldehyde (Taylor, E. C., Skotnicki, J. S. Synthesis, 1981, 606) (10 mmol, 2.44 g), sodium azide (30 mmol, 1.95 g) and triethylamine hydrochloride (30 mmol, 4.13 g) in toluene was heated to ˜95° C. over night (Koguro, K., Oga, T., Missui, S. and Orita, R. Synthesis, 1998, 910). After cooling the mixture was poured into water and the solid which was formed was collected. To the aqueous layer 36% hydrochloric acid was added dropwise to salt out more solid. The combined solids were dried to yield the title compound as an off-white solid (2.30 g, 80%); 1H NMR (300 MHz, DMSO-d6) δ 1.70 (t, J=5.7 Hz, 4 H), 3.44 (t, J=5.7 Hz, 4 H), 3.92(s, 4 H), 7.12(d, J=9.0 Hz, 2 H), 7.85(d, J=9.0 Hz, 2 H); MS (ES) m/z: 288.4 (MH+); HRMS Calcd. for C14H17N5O(M+): 287.1382. Found: 287.1375.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07022716B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-64eefa25e78a4ed597c0f36ab2dd91a5 |
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| Source note | uspto-grants-2006_04 |
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