HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → HCID 20262586, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 54060996 | HCID 54060996 | — |
| Product | HCID 20262586 | HCID 20262586 | — |
Reaction Steps
It is contemplated that the foregoing product by reaction with phosgene and ethyl chloroformate can be converted to N-(3-chloro-4-methoxyphenyl)isatoic anhydride [VIII; R=H, R"=3--Cl, OR°=4--OCH3 ], and the latter reacted with piperidine to give 1-[2-(3-chloro-4-methoxyphenylamino)benzoyl]piperidine [IX; R=H, R"=3--Cl, N=Z=1-piperidinyl, OR°=4--OCH3 ] which can be de-etherified with boron tribromide to yield 1-[2-(3-chloro-4-hydroxyphenylamino)benzoyl]piperidine [I; R and R'=H, R"=3--Cl, N=Z=1-piperidinyl, OH at 4-position].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510139 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-3541645e906b491286160c2604298121 |
| Source note | uspto-grants-1985_04 |