HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269733Generated: October 31, 2026
Hydrochloric Acid → 3,4,5,6-Tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid N'-pentanoyl-hydrazide
https://huagongshe.com/reaction/269733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Valerohydrazide | HCID 93202 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4,5,6-Tetrahydro-2H-[1,2']bipyridinyl-4-carboxylic acid N'-pentanoyl-hydrazide | HCID 23544070 | 30.6% |
Reaction Steps
The carboxylic acid from Preparation 2 (1.5 g, 7.3 mmol) was suspended in dichloromethane (40 mL) containing N,N-dimethylformamide (2 drops) and oxalyl chloride (1.27 mL, 14 mmol) in dichloromethane (5 mL) was added dropwise. The mixture was stirred for 5 hours at room temperature and then evaporated under reduced pressure. The residue was suspended in hexane and evaporate (3×20 mL). The residue was dissolved in dichloromethane and cooled to 0° C. and pentanoic acid hydrazide (1.7 g, 14.6 mmol) was added. 1-Methyl-pyrrolidin-2one (1.6 mL, 14.6 mmol) in dichloromethane (10 mL) was added drop wise and the mixture was stirred at room temperature for 16 hours. The solvent was evaporated under reduced pressure and the residue was triturated with diethyl ether. The material obtained was dissolved in water and acidified to pH 2 by addition of 2N hydrochloric acid. The acidic solution was filtered and the filtrate was washed with ethyl acetate (3×20 mL) then basified with sodium carbonate. The solid formed was triturated with diethyl ether and isolated by filtration to give the title compound as a white solid (0.68 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07449462B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-51cfafd6d26a4f528f49b7ab12cf7290 |
|---|
| Source note | uspto-grants-2008_11 |
|---|