Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 58659422 | HCID 58659422 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58659356 | HCID 58659356 | — |
Reaction Steps
A mixture of N-(4-(4-chloropyrimidin-6-yl-oxy)-phenyl)-N′-(3-trifluoromethyl-4-(piperidin-1-ylmethyl)-phenyl)-urea (Example 128; 350 mg, 0.69 mmol) and NaN3 (91 mg, 1.4 mmol) in 7 ml of DMF is stirred for 2 h at 70° C. The resulting mixture is concentrated in vacuo, the residue diluted with AcOEt and water, the aqueous layer separated off and extracted twice with AcOEt. The organic phases are washed with water and brine, dried (Na2SO4) and concentrated to yield the title compound: MS: [M+1]+=513.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652022B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-79c9074d9054428796011f93b203051a |
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| Source note | uspto-grants-2010_01 |
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