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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735710Generated: November 3, 2026

Ammonia → HCID 9824850, compound

https://huagongshe.com/reaction/1735710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAnisoleHCID 7519—
Reactant1-PiperonylpiperazineHCID 94426—
ReactantHCID 15428875HCID 15428875—
CatalystTitanium TetrachlorideHCID 24193—
SolventTolueneHCID 1140—
SolventIsopropanolHCID 3776—
ProductHCID 9824850HCID 982485070.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of anisole (0.40 mL, 3.68 mmol) in dry toluene (2.00 mL) was added titanium tetrachloride (0.24 mL, 2.18 mmol) at room temperature under argon. The mixture was then treated with 1-piperonylpiperazine (2.07 g, 9.40 mmol) and 4-chloro-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine (0.49 g, 2.00 mmol) (Giani et al, supra) and diluted with toluene (1.00 mL). After more 1-piperonylpiperazine (1.19 g, 5.40 mmol) was added, toluene (8.00 mL) was added and the resulted reaction mixture was heated at reflux for 6 h before it was cooled to 60° C. Isopropanol (0.80 mL), celite (0.40 g) and ammonia (30%, 0.50 mL) were added sequentially and the whole mixture was filtered hot. Upon cooling to room temperature, the filtrate was concentrated in vacuo to dryness and the residue was subjected to column chromatography using ethyl acetate/hexanes (1/2) as the eluent. Thus 0.63 g (70%) of the title compound was afforded as a light yellow solid; m.p. 160°-162° C; MS 447 (M+ +1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538965
Source datasetuspto-grants-1996_07
ORD IDord-8505de6268fd47aeb8f7f97a9c52153c
Source noteuspto-grants-1996_07