Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 24800094 | HCID 24800094 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 24800095 | HCID 24800095 | — |
Reaction Steps
A suspension of 3-[3-(4-chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid ethyl ester (30 mg, 0.064 mmol) (from Example 4 supra) in methyl sulfoxide (1 mL) and ethanolamine (3 mL) (Aldrich) was heated at 135° C. for 2 hours in a microwave reactor. After cooling to room temperature, the precipitate was filtered off, washed with MeOH and dried to give 3-[3-(4-chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid (2-hydroxy-ethyl)amide as a white solid. (Yield 13.2 mg, 42.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07994321B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-de7fd72b9d3340dd81dd19dc55e9125a |
|---|
| Source note | uspto-grants-2011_08 |
|---|