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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014272Generated: November 1, 2026

Diethylamine → HCID 59442033, compound

https://huagongshe.com/reaction/1014272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetyl chlorideHCID 89602—
Reactant5-methoxy-6-nitro-2,3-dihydro-1H-indoleHCID 59441656—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59442033HCID 59442033100%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-(methyloxy)-6-nitro-2,3-dihydro-1H-indole (Intermediate B99, 433 mg, 2.23 mol), bromoacetyl chloride (386 mg, 2.45 mmol) and K2CO3 (924 mg, 6.69 mmol) in THF (50 mL) was stirred for 40 min and then Et2NH (326 mg, 4.46 mmol) was added. The reaction mixture was stirred for 1 day, additional Et2NH (0.3 mL) was added, stirring was continued for an additional 24 h, then the reaction was heated at 60° C. for 2 h. The resulting mixture was diluted with EtOAc (200 mL), washed with water (150 mL) and a saturated NaCl solution (100 mL), and back extracted with EtOAc (100 mL). The organic layers were combined, dried (Na2SO4), and concentrated to obtain N,N-diethyl-2-[5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-2-oxoethanamine (687 mg, 100%). ESIMS (M+H)+=307.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-fa266c7a725c4ac2a3e0d096008477e7
Source noteuspto-grants-2011_07