Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 178437440 | HCID 178437440 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178437415 | HCID 178437415 | 79% |
Reaction Steps
A mixture of 5-Cyano-2-ethyl-7-methyl-3-(2'-(tetrazol-5-yl)biphen-4-yl)methyl-3H-imidazo[4,5-b]pyridine (54 mg), trimethylstannyl azide (79 mg), toluene (5 mL), and DMF (1 mL) was heated to 110° C. for 24 hour. Concentration and purification (SiO2, 70/30/1CH2Cl2 /MeOH/NH4OH) gave 47 mg solid. 1H NMR (300 MHz, CD3OD) δ 7.93 (s, 1H), 7.56-7.38 (m, 4H), 7.14-7.05 (AB quartet, 4H), 5.61 (s, 2H), 2.86 (q, H, J=7.5 Hz), 2.71 (s, 3H), 1.27 (t, 3H, J=7.5 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05332744 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-da5d09e0af6b41c1a75dda187387c5a3 |
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| Source note | uspto-grants-1994_07 |
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