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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482452Generated: October 28, 2026

Ammonia → HCID 9824850, compound

https://huagongshe.com/reaction/482452

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 numberUS05798350
Source datasetuspto-grants-1998_08
ORD IDord-768b3fc8a3b64ccc9b9f9c73f99e6b09
Source noteuspto-grants-1998_08