HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416213Generated: October 28, 2026
3-(Bromoacetyl)quinolin-2(1H)-one → HCID 10287694, compound
https://huagongshe.com/reaction/2416213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Bromoacetyl)quinolin-2(1H)-one | HCID 22638554 | — |
| Reactant | HCID 22638635 | HCID 22638635 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10287694 | HCID 10287694 | — |
Reaction Steps
A mixture of 3-(2-bromoacetyl)-1h-quinolin-2-one (Example 27(b), 270 mg, 1.0 mmol) and 2-amino-1,1-dimethyl-1-(phenylsulfonyl)ethane-2-thione (step b, 1.7 ml, 1.0 mmol) in 3.5 ml of anhydrous MeOH was heated at 120° C. for 5 min by microwave synthesizer. The reaction mixture was cooled to RT. The precipitates were collected by filtration and washed with MeOH and CH2Cl2 to provide the title compound as a light yellow solid. Ms m/z: 411.3 (m+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06822097B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-2981c4fc07134adfbf34dd3d34f01133 |
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| Source note | uspto-grants-2004_11 |
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