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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046168Generated: November 2, 2026

2-Methylpyridine-4-boronic acid → HCID 58109483, compound

https://huagongshe.com/reaction/1046168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylpyridine-4-boronic acidHCID 4192664—
ReactantHCID 66857463HCID 66857463—
ReactantHCID 66857543HCID 66857543—
ProductHCID 58109483HCID 58109483—

Reaction Steps

Isomer 1 of the title compound, (S)-6-(4-fluorophenyl)-6-methyl-3-((S)-1-(4-(2-methylpyridin-4-yl)phenyl)ethyl)-1,3-oxazinan-2-one, was prepared from (S)-3-((S)-1-(4-bromophenyl)ethyl)-6-(4-fluorophenyl)-6-methyl-1,3-oxazinan-2-one and 2-methylpyridine-4-boronic acid following a procedure analogous to that described in Example 14. LC-MS Method 1 tR=1.28, m/z=405 (M+1); 1H NMR (CDCl3) 8.84 (d, 1H, J=6.1 Hz), 7.81 (d, 1H, J=5.9 Hz), 7.75 (s, 1H), 7.70 (d, 2H, J=8.2 Hz), 7.52 (d, 2H, J=8.20 Hz), 7.34-7.31 (m, 2H), 7.09 (t, 2H, J=8.6 Hz), 5.81 (q, 1H, J=7.2 Hz), 2.89 (s, 3H), 2.84-2.72 (m, 2H), 2.31 (dt, 1H, J=13.9, 3.7 Hz), 2.11-2.03 (m, 1H), 1.64 (s, 3H), 1:38 (d, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-b014271142254b6da377276592b70101
Source noteuspto-grants-2013_10