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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615442Generated: November 1, 2026

(6-((tert-Butoxycarbonyl)amino)pyridin-3-yl)boronic acid → HCID 86680679, compound

https://huagongshe.com/reaction/1615442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-((tert-Butoxycarbonyl)amino)pyridin-3-yl)boronic acidHCID 54751702—
Reactanttert-butyl 5-((diphenoxyphosphoryl)oxy)-2H-1,4-oxazine-4(3H)-carboxylateHCID 86680661—
ProductHCID 86680679HCID 8668067926%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765751B2
Source datasetuspto-grants-2014_07
ORD IDord-7b31542fa4e54c0ea586ddc501ea4979
Source noteuspto-grants-2014_07