HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059278Generated: November 3, 2026
Trifluoroacetic acid → 8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine
https://huagongshe.com/reaction/1059278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 10-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine | HCID 11335363 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine | HCID 11747038 | 83.5% |
Reaction Steps
Into 250 ml of a solution of 26.9 g of 8-chloromethyl-10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazine in methylene chloride was dropped 50 ml of trifluoroacetic acid at 0° C. After reacting at room temperature for 12 hours, the reaction mixture was cooled to 0° C. and neutralized by adding an aqueous solution of sodium hydrogencarbonate. The crystals thus precipitated were taken up by filtration and washed successively with water and diethyl ether to thereby give 19.1 g of the title compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-a4fe67fb396c4809b613d57a387c8948 |
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| Source note | uspto-grants-2003_02 |
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