HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568341Generated: October 30, 2026
Acetyl chloride → HCID 20150309, compound
https://huagongshe.com/reaction/568341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20150296 | HCID 20150296 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20150309 | HCID 20150309 | — |
Reaction Steps
A solution of acetyl chloride (0.55 cc) in methylene chloride (5 cc) is added in the course of 10 minutes to a stirred solution of 4-[(6-amino-2-phenyl-4-quinolyl)oxyacetyl]morpholine (2.55 g), prepared according to Example 39, and triethylamine (1.2 cc) in methylene chloride (25 cc). The mixture is stirred for 1 hour at room temperature (approximately 20° C.) and the solvent evaporated off under reduced pressure. The residue is stirred for 10 minutes in an ethyl acetate/water (5:2 by volume) mixture, filtered off, dissolved in a toluene/acetic acid (50:50 by volume) mixture and precipitated with ethyl ether. After filtration and drying, 4-[(6-acetylamino-2-phenyl-4-quinolyl)oxyacetyl]morpholine (2 g), m.p. 261° C., is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04728647 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-6c886343ac3349fc911266c05cadb8dc |
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| Source note | uspto-grants-1988_03 |
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