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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514969Generated: October 30, 2026

Methyl morpholine oxide → HCID 73672704, compound

https://huagongshe.com/reaction/514969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 86716050HCID 86716050—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
ProductHCID 73672704HCID 7367270424%

Reaction Steps

To a solution of 2,3-dichloro-N-(2-(4-hydroxypiperidin-1-yl)-2-(2-methylpyrimidin-5-yl)ethyl)benzamide (130 mg, 0.32 mmol) in DCM (5 mL) was added 4 A molecular sieves (1.3 g), NMO (205 mg, 1.75 mmol) and TPAP (2.2 mg). The mixture was stirred at room temperature overnight. The resulting mixture was filtered. The filtrate was washed with water, dried over Na2SO4 and concentrated. The residue was purified by preparative TLC (EtOAc:MeOH=100:3) to give 2,3-dichloro-N-(2-(2-methylpyrimidin-5-yl)-2-(4-oxopiperidin-1-yl)ethyl)benzamide (31 mg, yield: 24%) as a white solid. 1HNMR (CDCl3 400 MHz): δ8.59 (s, 2H), 7.56 (dd, J=8.0 Hz, 1.6 Hz, 1H), 7.49 (dd, J=7.6 Hz, 1.6 Hz, 1H), 7.34-7.27 (m, 1H), 6.63 (br, 1H), 4.08-3.82 (m, 3H), 2.95-2.82 (m, 2H), 2.79-2.65 (m, 5H), 2.55-2.40 (m, 4H). LCMS (MH+): m/z=425.0, tR (minutes, Method F)=1.75

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108938B2
Source datasetuspto-grants-2015_08
ORD IDord-f8e9e37aa14940beaf9d9170b85d444e
Source noteuspto-grants-2015_08