HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-((tert-Butoxycarbonyl)amino)pyridin-3-yl)boronic acid → HCID 86680679, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-((tert-Butoxycarbonyl)amino)pyridin-3-yl)boronic acid | HCID 54751702 | — |
| Reactant | tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate | HCID 86680661 | — |
| Product | HCID 86680679 | HCID 86680679 | 26% |
Reaction Steps
This compound was prepared from tert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylate and 6-(tert-butoxycarbonylamino)pyridin-3-ylboronic acid using a procedure similar to that described in Example 2 (Steps 1-3a) above. The product was isolated as a white solid (26% yield); 1H-NMR (d6-DMSO) 1.10 (9H, s), 1.46 (9H, s), 3.69 (2H, t), 4.10 (2H, t), 6.43 (1H, s), 7.51-7.54 (1H, m), 7.73 (1H, m), 8.06 (1H, s), 9.75 (1H, s); 13C-NMR (d6-DMSO) 27.9, 28.3, 41.7, 66.8, 111.3, 132.3, 133.1, 135.0, 143.9; MS ES(+) 378.0 M++1); HRMS m/z calcd for C19H27N3O5+H+ 378.2029 [M+H+]. Found 378.2035. IR λmax=1699 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765751B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-7b31542fa4e54c0ea586ddc501ea4979 |
| Source note | uspto-grants-2014_07 |