HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797609Generated: October 31, 2026
2-Mercaptoacetamide → HCID 22175936, compound
https://huagongshe.com/reaction/1797609
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptoacetamide | HCID 12961 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22175497 | HCID 22175497 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22175936 | HCID 22175936 | 50% |
Reaction Steps
A solution (2 mL) of 2-mercaptoacetamide (0.27 g, 3.0 mmol) in N,N-dimethylformamide was ice-cooled under a nitrogen atmosphere and sodium hydride (0.12 g, 3.0 mmol) (60% in oil) was added thereto. The resulting mixture was stirred under ice-cooling for 30 min. To the obtained suspension was added 3-(aminomethyl)-6-bromo-2-isobutyl-4-phenyl-1(2H)-isoquinolinone (1.06 g, 2.74 mmol), and the mixture was stirred at 80° C. for 24 h. The reaction mixture was partitioned between water (100 mL) and ethyl acetate (50 mL), and the aqueous layer was extracted twice with ethyl acetate (50 mL). The extracts were combined and washed with saturated brine (20 mL), dried over anhydrous magnesium sulfate (12 g) and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=1:0–10:1 (v/v)) and recrystallized from n-hexane-ethyl acetate (1:1) to give the title compound (0.54 g, 50%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07034039B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-548f52ae06484d91bedb393b1cafb390 |
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| Source note | uspto-grants-2006_04 |
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