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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939174Generated: November 2, 2026

Methyl iodide → HCID 21467113, compound

https://huagongshe.com/reaction/1939174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-t-butyloxycarbonylamino-3,4-dihydro-1H-1-benzazepine-2,5-dioneHCID 14666414—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 21467113HCID 2146711378.3%

Reaction Steps

A solution of 3-tertbutyloxycarbonylamino-2,3,4,5-tetrahydro-2,5-dioxobenzo[b]azepine (5 g, 17.2 mmole) in DMF (50 mL) was treated with potassium carbonate (4.76 g, 34.4 mmole) and methyl iodide (4.88 g, 34.4 mmole). The reaction was stirred at ambient temperature for 4 hours. The mixture was diluted with ethyl acetate (300 ml) and saturated aqueous sodium hydrogen carbonate (500 ml). The organic layer was separated and the aqueous layer was extracted again with ethyl acetate (2×300 ml). The organic layers were combined, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resulting solid was swished with warm ethyl ether (200 mL) and collected by filtration to give 4.1 g of the product. mp 205°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696111
Source datasetuspto-grants-1997_12
ORD IDord-2fba4eab9f0549438b2d76d3fe60ee69
Source noteuspto-grants-1997_12