HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671515Generated: November 2, 2026
Ethanolamine → 3-[3-(3-Chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid (2-hydroxy-ethyl)-amide
https://huagongshe.com/reaction/1671515
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 3-[3-(3-Chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid ethyl ester | HCID 24800265 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-[3-(3-Chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid (2-hydroxy-ethyl)-amide | HCID 24178386 | — |
Reaction Steps
A suspension of 3-[3-(3-chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid ethyl ester (34.0 mg, 0.073 mmol) (from Example 10 supra) in methyl sulfoxide (1 mL) and ethanolamine (3 mL) (Aldrich) was heated at 135° C. for 2 hours in a microwave reactor. The solvent was removed in vacuum and the residue was treated with MeOH (2 mL). The resulting white precipitate was filtered, washed with cold MeOH and dried to give 3-[3-(3-chloro-benzoylamino)-phenoxymethyl]-thieno[3,2-c]pyridine-7-carboxylic acid (2-hydroxy-ethyl)-amide as a white solid. (Yield 25.7 mg, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994321B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8a8991820d504bb09fbfde52800db84a |
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| Source note | uspto-grants-2011_08 |
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