HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Cyanophenol → HCID 22613902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Cyanophenol | HCID 13394 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Cyanophenylboronic acid | HCID 2734325 | — |
| Reactant | Methyl 3-bromo-5-methylbenzoate | HCID 22613903 | — |
| Reactant | HCID 22613911 | HCID 22613911 | — |
| Product | HCID 22613902 | HCID 22613902 | — |
Reaction Steps
Analogously to Example 1, by reaction of 3-cyanophenylboronic acid with methyl 3-bromo-5-methylbenzoate the compound methyl 3′-cyano-5-methylbiphenyl-3-carboxylate is obtained. By bromination with NBS and reaction with 3-hydroxybenzonitrile, methyl 3′-cyano-5-(3-cyanophenoxymethyl)biphenyl-3-carboxylate is obtained. Reaction with hydroxylamine and reduction using H2/Raney Ni affords the compound methyl 3′-carbamimidoyl-5-(3-carbamimidoylphenoxymethyl)biphenyl-3-carboxylate. By hydrolysis of the ester with aqueous NaOH, 3′-carbamimidoyl-5-(3-carbamimidoylphenoxymethyl)biphenyl-3-carboxylic acid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380430B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-1ccbfff1cc9d445e9f849fa762c63cfe |
| Source note | uspto-grants-2002_04 |