HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080212Generated: November 2, 2026
Water → 2-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide
https://huagongshe.com/reaction/2080212
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(Ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130432 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Methylamino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide | HCID 23130696 | 67% |
Reaction Steps
To a solution of 2-(ethoxymethyl-amino)-N-(5-phenoxy-thiophene-2-ylmethyl)-nicotinamide described in Preparation Example A+-6 (148 mg, 0.385 mmol) in dimethylsulfoxide (3 mL) was added sodium borohydride (44 mg, 1.15 mmol), and the solution was stirred for 30 minutes at 100° C., followed by stirring for 20 minutes at 110° C. Furthermore, sodium borohydride (35 mg, 0.925 mmol) was added thereto, followed by stirring for 20 minutes at 110° C. Water was added to the reaction mixture, which was then extracted with ethyl acetate, the organic layer was sequentially washed with water and brine, dried over anhydrous sodium sulfate, and then, concentrated in vacuo. The obtained residue was purified by silica gel chromatography (hexane-ethyl acetate), and the title compound (86 mg, 0.26 mmol, 67%) was obtained.
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-678f674f3e75494cb9068c34d2c9f122 |
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| Source note | uspto-grants-2011_04 |
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