HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Fluoro-2-nitrobenzene → 2-Fluorodibenzo[B,F][1,4]thiazepin-11(10H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | [2-(4-Fluoro-phenylsulfanyl)-phenyl]-carbamic acid phenyl ester | HCID 67079783 | — |
| Reactant | 1-Amino-2-phenylsulfanyl-(4-fluorobenzene) | HCID 67256766 | — |
| Product | 2-Fluorodibenzo[B,F][1,4]thiazepin-11(10H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653257B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-968f2e6370f546a1bd879a2e8fdc322c |
| Source note | uspto-grants-2014_02 |