HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49378Generated: October 27, 2026
Acetamidine monohydrochloride → HCID 178432569, compound
https://huagongshe.com/reaction/49378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamate | HCID 12986050 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178432569 | HCID 178432569 | 67.1% |
Reaction Steps
Acetamidine hydrochloride (112 mg, 1.18 mmol), benzyl-[2-(4-bromoacetyl-phenoxy)-ethyl]-carbamate (160 mg, 0.39 mmol), and sodium ethoxide (80.3 mg, 1.18 mmol) were combined in a round-bottomed flask, dissolved in ethanol, and heated to about 80° C. for about two hours. The reaction mixture was then allowed to cool to room temperature, and the resulting heterogenous mixture was filtered. The filtrate was then concentrated in vacuo to an oil which was purified by column chromatography (silica gel; 5% methanol/methylene chloride to 10% methanol/methylene chloride) to afford 92 mg (64% yield) of the desired product. LRMS ([M+H]+)=352.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706743B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-fe29b5ff1a114e16a240a8f32959a868 |
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| Source note | uspto-grants-2004_03 |
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