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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519479Generated: November 4, 2026

Dimethylformamide → HCID 91074791, compound

https://huagongshe.com/reaction/1519479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl N-methylaminoacetate hydrochlorideHCID 171173—
ReactantHCID 25134204HCID 25134204—
SolventWaterHCID 962—
ProductHCID 91074791HCID 9107479153.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

{7-Chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} chloroacetate (500 mg, 0.95 mmol), ethyl sarcosinate hydrochloride (230 mg, 1.5 mmol), and potassium carbonate (414 mg, 3.0 mmol) were added to dimethylformamide (DMF) (5 ml), and the mixture was stirred at 60° C. for 1 hour. Water was added to the reaction mixture, and the resulted precipitates were collected by filtration and washed with water. The precipitates were dissolved in ethyl acetate, dried over anhydrous sodium sulfate, filtrated and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=36:64→15:85). The purified product was concentrated under reduced pressure. Water was added the residue, and resulted precipitates were collected by filtration and dried to obtain 330 mg of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (ethoxycarbonylmethyl-methyl-carbamoyloxy)acetate as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073868B2
Source datasetuspto-grants-2015_07
ORD IDord-66b0dc063d0c42e8b917e5f50fd6a6f9
Source noteuspto-grants-2015_07