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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366793Generated: October 30, 2026

4-Methylmorpholine → HCID 86755935, compound

https://huagongshe.com/reaction/366793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 3815830HCID 3815830—
ReactantHCID 23289852HCID 23289852—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86755935HCID 8675593575.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

(8-Chloro-6,11-dihydro-6-methyl-5H-pyrido[3,2-c][1]benzazepin-11-yl)-piperazine (100 mg, 0.305 mmol), 4-pyridine-acetic acid 1-oxide (93.3 mg, 0.61 mmol), EDCl (0.116 g, 0.61 mmol) and HOBT (82.4 mg, 0.61 mmol) were dissolved in DMF (2 ml), and NMM (1 ml) was added. The reaction mixture was stirred at 20° C. for 18 hours and then diluted with water (50 ml), and the aqueous phase was then extracted with EtOAc (about 8 times) until no product was visible in the aqueous layer. The EtOAc phase was then washed with aqueous Na2CO3 and chromatographed on silica gel to afford the title compound (107 mg), m.p. 115-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130229
Source datasetuspto-grants-2000_10
ORD IDord-845aaa796a7c49cd8740b3eb5c6dbdbd
Source noteuspto-grants-2000_10