HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514969Generated: October 30, 2026
Methyl morpholine oxide → HCID 73672704, compound
https://huagongshe.com/reaction/514969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 86716050 | HCID 86716050 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73672704 | HCID 73672704 | 24% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108938B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f8e9e37aa14940beaf9d9170b85d444e |
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| Source note | uspto-grants-2015_08 |
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