HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-(5-Methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid → 1'-Ethyl-5-[4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carbonyl]-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-(5-Methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid | HCID 18797043 | — |
| Reactant | 1'-Ethyl-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine] | HCID 21833744 | — |
| Product | 1'-Ethyl-5-[4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carbonyl]-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine] | HCID 21833822 | 31% |
Reaction Steps
The title compound was prepared from 4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid (D11) and 1'-ethyl-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine] (D109) using a similar procedure as that outlined in Example 1, to afford the title compound as a yellow gum (31%). This was converted to its hydrochloride salt to yield an off white solid m.p. 245-249° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05972951 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-1efe16ea59e2420ab79da6e6c297a9d5 |
| Source note | uspto-grants-1999_10 |