HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluorobenzyl chloride → HCID 19907879, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Reactant | 2,3-Diaminopyridine | HCID 9956 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19907879 | HCID 19907879 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 3 parts of 2,3-pyridinediamine and 4 parts of 1-(chloromethyl)-4-fluorobenzene was stirred overnight at 120° C. Trichloromethane and a dilute ammonium hydroxide solution were added and the product was extracted. The organic phase was washed with water, dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The second fraction was collected and the eluent was evaporated, yielding 1.8 parts of N3 -[(4-fluorophenyl)methyl]-2,3-pyridinediamine as a residue (intermediate 18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE033833 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-f6f6122aada1421cb0ac38b963acb7ba |
| Source note | uspto-grants-1992_02 |