HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14099442, compound → HCID 14099441, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14099442 | HCID 14099442 | — |
| Reactant | HCID 14099443 | HCID 14099443 | — |
| Product | HCID 14099441 | HCID 14099441 | — |
Reaction Steps
Following the procedure described in Example 38 but using a molar equivalent quantity of the appropriate 3- and 4-hydroxypiperidine in place of 1,4-dioxa-8-azaspiro[4,5]decane one obtains the suitably substituted γ-oxobenzenebutanoic acids which upon cyclization with hydrazine gives the following compounds: 37b. 4,5-dihydro-6-[4-(4-hydroxy-1-piperidinyl)phenyl]-3(2H)-pyridazinone, mp 262°-263° C. 37c. 4,5-Dihydro-6-[4-(3-hydroxy-1-piperdinyl)phenyl)-3(2H)-pyridazinone, mp 211°-212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04734415 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-43332e2d23bf4a16bd2214445e78f2d5 |
| Source note | uspto-grants-1988_03 |