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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248249Generated: October 30, 2026

Tetrahydrofuran → HCID 12852074, compound

https://huagongshe.com/reaction/1248249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 20278962HCID 20278962—
ProductHCID 12852074HCID 1285207430%

Reaction Steps

A mixture of 2.2 parts of 2-amino-4-fluoro-N-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]benzamide, 1.2 parts of 1,1'-bis[1H-imidazol-1-yl]methanone and 45 parts of tetrahydrofuran is stirred and refluxed for 3 hours. The reaction mixture is cooled and the solvent is evaporated. The residue is boiled in 4-methyl-2-pentanone. The solid product is filtered off and crystallized from N,N-dimethylformamide, yielding 0.8 parts (30%) of 7-fluoro-3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione; mp. 248° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522945
Source datasetuspto-grants-1985_06
ORD IDord-5a1dc2062d3448dd8c48ae4064c001a3
Source noteuspto-grants-1985_06