HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383645Generated: October 25, 2026
4-(Pyrrolidin-1-yl)phenacyl bromide → HCID 59406739, compound
https://huagongshe.com/reaction/383645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Pyrrolidin-1-yl)phenacyl bromide | HCID 3681785 | — |
| Reactant | Ethyl[3-(6-oxo-3-thiocarbamoyl-6h-pyridazin-1-yl-methyl)phenyl]carbamate | HCID 59406698 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59406739 | HCID 59406739 | — |
Reaction Steps
104 mg (0.31 mmol) of ethyl[3-(6-oxo-3-thiocarbamoyl-6H-pyridazin-1-yl-methyl)phenyl]carbamate are suspended in 2 ml of EtOH, and 100 mg (0.37 mmol) of α-bromo-4-(1-pyrrolidino)acetophenone are added. The reaction mixture is stirred at 80° C. for 15 h. The precipitate formed is filtered off with suction and washed with ethanol and dried in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367668B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-aa239a8cb89b42f0a6711a235c785e39 |
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| Source note | uspto-grants-2013_02 |
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