HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylhydrazinecarbothioamide → 2-[4-Chloro-1-(pyridin-3-yl)-butylidene]-N-methyl-hydrazinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylhydrazinecarbothioamide | HCID 2723853 | — |
| Reactant | 4-Chloro-1-(pyridin-3-YL)butan-1-one | HCID 12471005 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[4-Chloro-1-(pyridin-3-yl)-butylidene]-N-methyl-hydrazinecarbothioamide | HCID 54474414 | 112.2% |
Reaction Steps
A mixture of 4-chloro-1-(3-pyridinyl)-1-butanone (4.4 g, 24 mmol) and 4-methylthiosemicarbazide (2.5 g, 24 mmol) in 150 mL of ethanol under a nitrogen atmosphere was warmed to dissolve all the solids and then allowed to stir at room temperature overnight. By TLC the reaction was not complete. The reaction was then heated at 70° C. for 5 hours and overnight at room temperature. The solvent was removed under reduced pressure to give 7.29 g of a yellow oil. Purification of this oil on 700 g of silica gel (230-400 mesh) using 50-70% EtOAc-hexane as the eluent gave 4.14 g (64%) of the title compound as a white solid, mp 100-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008362 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-0b3210bde09d4528a1999574f3a04593 |
| Source note | uspto-grants-1999_12 |