HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630808Generated: October 30, 2026
Hexachloroethane → [1-(6-Fluoro-[1,2,4]triazolo[4,3-a]pyridin-3-yl)-1-methyl-ethyl]-dimethyl-amine
https://huagongshe.com/reaction/630808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexachloroethane | HCID 6214 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Dimethylamino-2-methyl-propionic acid N'-(5-fluoro-pyridin-2-yl)-hydrazide | HCID 86687093 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(6-Fluoro-[1,2,4]triazolo[4,3-a]pyridin-3-yl)-1-methyl-ethyl]-dimethyl-amine | HCID 89624176 | 85% |
Reaction Steps
To a solution of Intermediate 76a (195 mg, 0.81 mmol), Ph3P (426 mg, 1.62 mmol) and Et3N (452 □L, 3.25 mmol) in THF (9.00 mL) at 0° C. was added hexachloroethane (385 mg, 1.62 mmol). The reaction was stirred at RT overnight then partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (3×). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated in vacuo. The residue was dissolved in MeOH and loaded onto an SCX-2 cartridge, which was washed with MeOH and eluted with 2M NH3 in MeOH. The reaction showed 50% conversion so was re-submitted to the reaction conditions overnight at 50° C. The workup and purification procedures were repeated to give the title compound (153 mg, 85%). 1H NMR (300 MHz, CDCl3): 1.60 (6H, s), 2.20 (6H, s), 7.16 (1H, ddd, J 9.9, 7.4, 2.4), 7.71 (1H, ddd, J 9.9, 5.0, 0.8), 8.89 (1H, ddd, J 4.4, 2.4, 0.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09315503B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-b7f0a7f58bf442afa465b419a3f93601 |
|---|
| Source note | uspto-grants-2016_04 |
|---|