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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243527Generated: October 31, 2026

1-Fluoro-2-nitrobenzene → 2-Fluorodibenzo[B,F][1,4]thiazepin-11(10H)-one

https://huagongshe.com/reaction/243527

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant[2-(4-Fluoro-phenylsulfanyl)-phenyl]-carbamic acid phenyl esterHCID 67079783—
Reactant1-Amino-2-phenylsulfanyl-(4-fluorobenzene)HCID 67256766—
Product2-Fluorodibenzo[B,F][1,4]thiazepin-11(10H)-oneHCID 58015269—

Reaction Steps

Thus, 1-chloro-2-nitrobenzene may be reacted with 4-fluorobenzenethiol in the presence of a base to form 1-nitro-2-phenylsulfanyl-(4-fluorobenzene). The nitrofluorobenzene may be reduced to 1-amino-2-phenylsulfanyl-(4-fluorobenzene) which can converted (for example, as shown) to [2-(4-fluoro-phenylsulfanyl)-phenyl]-carbamic acid phenyl ester. Such an ester may be cyclized as shown to form 2-fluoro-10H-dibenzo[b,f][1,4]thiazepin-11-one, that may be converted to 11-chloro-2-fluoro-dibenzo[b,f][1,4]thiazepine, which can then be reacted with piperazine to form the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653257B2
Source datasetuspto-grants-2014_02
ORD IDord-968f2e6370f546a1bd879a2e8fdc322c
Source noteuspto-grants-2014_02