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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406705Generated: October 29, 2026

4-Iodo-1-methylpyridin-2(1H)-one → (R)-6-ethyl-3-((S)-1-(4-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)phenyl)propyl)-6-phenyl-1,3-oxazinan-2-one

https://huagongshe.com/reaction/406705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Iodo-1-methylpyridin-2(1H)-oneHCID 53408009—
Reactant(R)-3-((S)-1-(4-bromophenyl)propyl)-6-ethyl-6-phenyl-1,3-oxazinan-2-oneHCID 66600686—
Product(R)-6-ethyl-3-((S)-1-(4-(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)phenyl)propyl)-6-phenyl-1,3-oxazinan-2-oneHCID 59635810—

Reaction Steps

The title compound was prepared from (R)-3-((S)-1-(4-bromophenyl)propyl)-6-ethyl-6-phenyl-1,3-oxazinan-2-one following procedures analogous to those described in Example 32 Method 2 Steps 3 and 4 using 4-iodo-1-methylpyridin-2(1H)-one in Step 4. LC-MS Method 1 tR=1.58 min, m/z=431 (M+1); 1H NMR (CDCl3) 7.33 (1H, d, J=7.03 Hz), 7.29-7.21 (7H, m), 7.01 (2H, d, J=8.20 Hz), 6.75 (1H, d, J=2.05), 6.39 (1H, dd, J=2.05, 7.03), 5.48 (1H, ap dd, J=6.44, 9.66), 3.58 (3H, s), 2.95-2.87 (1H, m), 2.37-2.14 (3H, m), 2.06-1.81 (m, 4H), 1.00 (3H, t, J=7.32), 082 (3H, t, J=7.61).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754076B2
Source datasetuspto-grants-2014_06
ORD IDord-8626149f384e47c89493799ffc3bb2b0
Source noteuspto-grants-2014_06