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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272689Generated: October 31, 2026

2-Pyridone → HCID 69216827, compound

https://huagongshe.com/reaction/272689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridoneHCID 8871—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantHCID 69216097HCID 69216097—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69216827HCID 6921682737.9%

Reaction Steps

A mixture of Example 204A (150 mg, 0.52 mmol), pyridin-2 (1H)-one (96 mg, 1.0 mmol), PPh3 (180 mg, 0.68 mmol) and di-tert-butyl azodicarboxylate (160 mg, 0.68 mmol) in 10 mL of THF was stirred overnight. The reaction mixture was purified by flash column chromatography on silica gel with 7:3 hexanes/ethyl acetate to provide 72 mg of the desired product. The column was then washed with 100:3:1 EtOAc/MeOH/NH4OH to give 79 mg of 3-chloro-8-[2-(2-oxo-2H-pyridin-1-yl)-ethyl]-5,10-dihydro-dibenzo[b,e][1,4]diazepin-11-one. MS (DCI) m/e 366 (M+H)+; 1H NMR (500 MHz, DMSO-d6) δ 9.83 (s, 1H), 8.13-8.14 (m, 1H), 7.97 (s, 1H), 7.65-7.68 (m, 2H), 7.05 (d, J=1.84 Hz, 1H), 6.89-6.95 (m, 5H), 6.76 (d, J=8.42 Hz, 1H), 4.38 (t, J=6.86 Hz, 2H), 2.99 (t, J=6.86 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456169B2
Source datasetuspto-grants-2008_11
ORD IDord-568ee5f0294649de9d0856ed6c833041
Source noteuspto-grants-2008_11