Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Azide | HCID 33558 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | HCID 135948832 | HCID 135948832 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178518580 | HCID 178518580 | — |
Reaction Steps
To a suspension of Example 95A (150 mg) and trimethylsily azide (582 mg) in toluene (20 ml) was added dibutyltin oxide (28 mg). The mixture was heated at 100° C. for 3 days. Solid material was collected by filtration, washed with methanol and dried to give Example 95. Yield: 100 mg. MS (DCI/NH3) m/z 402 (M+H)+; 1H NMR (500 MHz, CD3OD): δ 1.81 (s, 2H), 1.92 (m, 1H), 2.02-2.11 (m, 1H), 2.35-2.44 (m, 4H), 2.51 (m, 2H), 2.91 (br s, 2H), 3.84-3.90 (m, 1H), 5.37 (br s, 1H), 5.51 (s, 2H), 5.51 (s, 2H), 7.30 (m, 2H), 7.97 (m, 2H),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546368B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-dc99d22a6d6c453eb4fbc5e78ef4ab92 |
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| Source note | uspto-grants-2013_10 |
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