HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620500Generated: October 30, 2026
2-Chloropyrimidine → HCID 13588090, compound
https://huagongshe.com/reaction/620500
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-[1-(2-aminoethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine | HCID 12891741 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13588090 | HCID 13588090 | 61% |
Reaction Steps
A mixture of 34.5 parts of 2-chloropyrimidine, 110 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine, 25 parts of sodium hydrogen carbonate and 1200 parts of ethanol was stirred and refluxed overnight. The reaction mixture was cooled and filtered over Hyflo. The filtrate was evaporated. The residue was purified by HPLC over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 82 parts (61%) of 1-[(4-fluorophenyl)methyl]-N-[1-[2-[(2-pyrimidinyl)amino]-ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine; mp. 168.4° C. (compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04820822 |
|---|
| Source dataset | uspto-grants-1989_04 |
|---|
| ORD ID | ord-33ca10973ff343208c5fe240fd19adb9 |
|---|
| Source note | uspto-grants-1989_04 |
|---|