HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(2-Fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-(Chloromethyl)-2-fluoropyridine | HCID 10844513 | — |
| Reactant | HCID 178524460 | HCID 178524460 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acid | HCID 23094028 | 53% |
Reaction Steps
A solution of triethylamine (7.0 mL, 50 mmol) in N,N-dimethylformamide (20 mL) was added to a solution of 4-chloromethyl-2-fluoropyridine (Reference compound No. 1-1, 5.5 g, 38 mmol) and 2-mercaptonicotinic acid (6.2 g, 40 mmol) in N,N-dimethylformamide (40 mL) under ice-cooling, then the mixture was stirred for 12 hours at room temperature. Ethyl acetate (50 mL) was added to the reaction mixture, the whole was extracted with 0.1 N aqueous sodium hydroxide solution (100 mL). 1 N hydrochloric acid was added to the aqueous layer to adjust to pH 5, and the precipitated crystal was filtered off. The crystal was dried at 80° C. under reduced pressure to give 5.3 g of the title reference compound as a brown solid. (Yield 53%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544703B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-8bfc315ed49242ea8f2cc19586117642 |
| Source note | uspto-grants-2009_06 |