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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473936Generated: October 30, 2026

N-Methylacetamide → HCID 67997198, compound

https://huagongshe.com/reaction/473936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylacetamideHCID 6582—
Reactant2,6-LutidineHCID 7937—
ReactantOxalyl chlorideHCID 65578—
Reactant4-{(S)-1-[(S)-6-(2-Hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazideHCID 66858074—
SolventDichloromethaneHCID 6344—
ProductHCID 67997198HCID 67997198—

Reaction Steps

2,6-Lutidine (88 μL) followed by oxalyl chloride (32 μL) was added to a solution of N-methyl-acetamide (28 mg) in dichloromethane (3 mL) chilled in an ice bath. After stirring the solution for 15 min, 4-{(S)-1-[(S)-6-(2-hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-benzoic acid hydrazide (154 mg) was added and then the cooling bath was removed. The solution was stirred for 1 h and then neutralized by the addition of saturated aqueous NaHCO3 solution. The resulting mixture was extracted twice with dichloromethane and the combined extracts were dried (MgSO4) and concentrated. The residue was taken up in acetic acid (1 mL) and stirred at 120° C. for 2.5 h. After cooling to ambient temperature, the solution was concentrated under reduced pressure and the residue was purified by chromatography on silica gel (CH2Cl2/MeOH 98:2->95:5) to afford pure Example 3 and a mixture containing Example 2. Example 2 was separated by a second chromatography on silica gel (CH2Cl2/MeOH 92:8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637505B2
Source datasetuspto-grants-2014_01
ORD IDord-0b75ff2a941d4d3d8804aa4053acd41d
Source noteuspto-grants-2014_01