HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080220Generated: November 1, 2026
Water → 6-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide
https://huagongshe.com/reaction/2080220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(Ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130345 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130424 | 48.1% |
Reaction Steps
To a solution of 6-(ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide described in Example A-153 (427 mg, 0.92 mmol) in dimethylsulfoxide (5 mL) was added sodium borohydride (100 mg, 2.7 mmol), and the solution was stirred for 15 minutes at 100° C. Water and ethyl acetate were added to the reaction solution, which was then partitioned, and the organic layer was washed with water three times. Silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, and purified by silica gel column chromatography (ethyl acetate). The solvent was evaporated in vacuo, hexane, diethyl ether and ethyl acetate were added to the residue for solidification, and the title compound (150 mg, 0.44 mmol, 48.1%) was obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932272B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-20a107388aeb44fa82aa02c21a050665 |
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| Source note | uspto-grants-2011_04 |
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