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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442385Generated: October 30, 2026

1-Chloro-2-nitrobenzene → HCID 21414420, compound

https://huagongshe.com/reaction/442385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantHCID 21414399HCID 21414399—
ProductHCID 21414420HCID 21414420—

Reaction Steps

By analogous procedures as in Examples 6 and 10, using the corresponding starting materials, 2-amino-5-fluorophenyl 1-methyl-4-piperidyl ketone is prepared and reacted with o-chloronitrobenzene to give 5-fluoro-2-(o-nitroanilino)-phenyl 1-methyl-4-piperidyl ketone. This intermediate is then reduced and cyclized in the presence of an acidic catalyst to give 2-fluoro-11-(1-methyl-4-piperidyl)-5H-dibenzo-[b,e][1,4]diazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045445
Source datasetuspto-grants-1977_08
ORD IDord-4c478406c3d04414b884b28888bf5a9f
Source noteuspto-grants-1977_08