HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Trimethylpyridine → N-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Thiomorpholine | HCID 67164 | — |
| Reactant | N-[(4-chlorophenyl)methyl]-2-(hydroxymethyl)-7-methyl-4-oxo-thieno[2,3-b]pyridine-5-carboxamide | HCID 6482399 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[(4-chlorophenyl)methyl]-7-methyl-4-oxo-2-(thiomorpholinomethyl)thieno[2,3-b]pyridine-5-carboxamide | HCID 6482405 | 60% |
Reaction Steps
To a solution of N-(4-chlorobenzyl)-2-(hydroxymethyl)-7-methyl-4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamide (0.300 g) from Example No. 35 in DMF (16 mL) are added DMAP (16 mg), 2,4,6-collidine (0.27 mL), and methanesulfonyl chloride (0.16 mL). The reaction mixture is stirred at room temperature for 2 h and then thiomorpholine (0.83 mL) is added. The mixture is stirred at room temperature for 3 d and is then poured into water (50 mL). The resulting off-white solid is filtered off and recrystallized from ethanol to yield 0.222 g (60%) of the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06239142B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-4ca572de4d224123b840374e88ef34e1 |
| Source note | uspto-grants-2001_05 |