HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → 3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Phenoxybenzoic acid | HCID 75182 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 2-(Hydroxy-(4-phenoxyphenyl)methylene)propanedinitrile | HCID 22347155 | — |
| Product | 3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carbonitrile | HCID 22346784 | — |
Reaction Steps
First, 4-amino-3-(4-phenoxyphenyl)-1H-pyrazole[3,4-d]pyrimidine may be prepared in accordance with procedures described in WO 2008/039218, for instance by converting 4-phenoxybenzoic acid to the corresponding acyl chloride (by using thionyl chloride), which latter product may be reacted with malononitrile to prepare 1,1-dicyano-2-hydroxy-2-(4-phenoxyphenyl)ethene. The methoxy moiety is then methylated using trimethylsilyldiazomethane, and that methylated product is the treated with hydrazine hydrate to provide 3-amino-4-cyano-5-(4-phenoxyphenyl)pyrazole, which is reacted with formamide to provide 4-amino-3-(4-phenoxyphenyl)-1H-pyrazole[3,4-d]pyrimidine, as illustrated in the following scheme:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156847B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-a7d1086aa96e4c3f8bf91b263dfca458 |
| Source note | uspto-grants-2015_10 |