HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892623Generated: October 30, 2026
Chloroacetyl chloride → HCID 131716539, compound
https://huagongshe.com/reaction/892623
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 9991469 | HCID 9991469 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 131716539 | HCID 131716539 | 56% |
Reaction Steps
Chloroacetyl chloride (2.2 g) was added dropwise to a mixture of 2-phenyl-5,6,7,8-tetrahydro-4H-thiazolo[5,4-b]azepine (3.0 g), triethylamine (3.6 ml) and methylenechloride (100 ml) under ice-cooling and stirring. After stirring for 30 mins. at room temperature, the mixture was distilled under reduced pressure to remove the solvent, and the residue was extracted with chloroform. The extract was washed with a saturated sodium hydrogen carbonate solution, water, dried over anhydrous sodium sulfate and the solvent removed by distillation under reduced pressure to give a crude product (4.0 g). To a solution of the above product (1.9 g) and triethylamine (2.6 ml) in 20 ml of THF was added N-methylpiperazine (1.4 ml), and the whole was stirred for 5 hrs. at room temperature. The reaction mixture was concentrated and extracted with ethyl ether. The extract was washed with water, dried and concentrated under reduced pressure. The residue was purified by a column chromatography on silica gel, converted into a salt of hydrochloric acid and then recrystallized from a mixture of isopropanol and ethyl ether to give the title compound (1.66 g, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05118806 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-1fe80b4cdd9e42bc8dbd8698cc92831c |
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| Source note | uspto-grants-1992_06 |
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