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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250256Generated: October 30, 2026

Tetrahydrofuran → 2(1h)-Quinazolinone,3,4-dihydro-8-methoxy-3-[1-(phenylmethyl)-4-piperidinyl]-

https://huagongshe.com/reaction/2250256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant(2-Amino-6-methoxy-benzyl)-(1-benzyl-piperidin-4-yl)-amineHCID 21102118—
Product2(1h)-Quinazolinone,3,4-dihydro-8-methoxy-3-[1-(phenylmethyl)-4-piperidinyl]-HCID 2110215668%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of (2-amino-6-methoxy-benzyl)-(1-benzyl-piperidin-4-yl)-amine (0.2 g, 0.62 mmol) in tetrahydrofuran (3 mL) at 0° C. was treated with carbonyl diimidazole (99 mg, 0.62 mmol). The reaction was stirred for 30 min at 0° C. and at reflux for 1 h. After cooling to room temperature, the solvent was evaporated and the residue purified by column to afford 150 mg (68%) of the desired product. LC/MS: tR=1.41 min, 352.30 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314883B2
Source datasetuspto-grants-2008_01
ORD IDord-27048f352e314ff8937a94abba216b22
Source noteuspto-grants-2008_01