HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(chloromethyl)-N-cyclopropylpyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-cyclopropyl-4-(hydroxymethyl)pyridine-2-carboxamide | HCID 59848863 | — |
| Product | 4-(chloromethyl)-N-cyclopropylpyridine-2-carboxamide | HCID 66631412 | — |
Reaction Steps
2.5 g (13.01 mmol) of N-cyclopropyl-4-(hydroxymethyl)pyridine-2-carboxamide (Example 52A) and 11.76 g (98.84 mmol) of thionyl chloride were combined and stirred at RT overnight. The reaction mixture was concentrated using a rotary evaporator. The residue was dissolved in ethyl acetate and washed once with saturated aqueous sodium bicarbonate solution. The organic phase was dried over magnesium sulfate, filtered and concentrated using a rotary evaporator. The residue was purified by column chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 2/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187428B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-62cf7e5595bb49c9ad538e15a1ea5daf |
| Source note | uspto-grants-2015_11 |