HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937415Generated: November 1, 2026
Benzyl Chloride → N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine
https://huagongshe.com/reaction/1937415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N2,N4,N4-trimethyl-N2-(4-piperidinyl)-2,4-pyrimidinediamine | HCID 53854017 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine | HCID 57066986 | 55.4% |
Reaction Steps
A mixture of chloromethylbenzene (1.9 g), intermediate 2 (3 g) and triethylamine (2.62 g) in N,N-dimethylacetamide (55 ml) was stirred for 2 hours at 75° C. The reaction mixture was poured out into ice-water and extracted with toluene. The separated organic layer was washed three times with water, dried, filtered and the solvent evaporated. The residue was dissolved in boiling petroleum ether and treated with activated charcoal. The mixture was filtered warm over dicalite, and the filtrate was concentrated. The concentrate was cooled on an ice-bath and the resulting precipitate was filtered off and dried, yielding 2.3 g (54.4%) of N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06395742B1 |
|---|
| Source dataset | uspto-grants-2002_05 |
|---|
| ORD ID | ord-39e5f7c0c7a04a6b8f610113f81985dc |
|---|
| Source note | uspto-grants-2002_05 |
|---|