Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244379Generated: October 31, 2026

Methyl iodide → HCID 86665015, compound

https://huagongshe.com/reaction/244379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86665014HCID 86665014—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86665015HCID 8666501583.7%

Reaction Steps

To a solution of the obtained 2-methyl-2-propanyl (3R)-3-[({4-[2-(dibenzylamino)ethyl]-2-(hydroxymethyl)-2,7-dimethyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-6-yl}carbonyl)(2-propanyl)amino]-1-piperidine carboxylate (22.5 g) in N,N-dimethylformamide (80 ml) were added sodium hydride (1.6 g) and methyl iodide (5.5 g) under ice-cooling. The mixture was stirred for 30 minutes, and then, cooled to room temperature, and further stirred for 2 hours. To the reaction solution was added a saturated aqueous ammonium chloride solution, and the mixture was ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, and dried over sodium sulfate. The sodium sulfate was removed by filtration, and the filtrate was concentrated under reduced pressure, followed by purification with silica gel chromatography to give the title compound (19.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658639B2
Source datasetuspto-grants-2014_02
ORD IDord-db9a4a0f103c4631bfe03b98b5bf4659
Source noteuspto-grants-2014_02