HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851005Generated: October 25, 2026
Chlorotrimethylsilane → 7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
https://huagongshe.com/reaction/851005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Acetyl-L-alanine | HCID 88064 | — |
| Reactant | 7-Amino-4-hydroxyquinoline-3-carboxylic acid | HCID 10262322 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid | HCID 13136876 | 62.7% |
Reaction Steps
A mixture of 3.93 g (30 mmol) of N-acetyl-L-alanine, 3.30 ml (30 mmol) of N-methyl morpholine, 2.33 ml (30 mmol) of methyl chloroformate, and 80 ml of acetonitrile is stirred at -10° to -20° for 30 minutes. A mixture of 4.08 g (20 mmol) of 7-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 8.4 ml (60 mmol) of triethylamine, 7.6 ml (60 mmol) of chlorotrimethylsilane, and 100 ml of dichloromethane is stirred at room temperature for 30 minutes and then cooled to -20°. The cold mixed anhydride is added to the cold silylated quinoline and stirred with cooling for 3 hours and overnight at room temperature. The reaction mixture is evaporated to dryness and the residue is treated with water. The solid is filtered to give 3.98 g of 7-[[2-(acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382089 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-f223e7d94c4c4fdab919dac0959f113f |
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| Source note | uspto-grants-1983_05 |
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