HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494410Generated: October 26, 2026
Riluzole → 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline
https://huagongshe.com/reaction/1494410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Riluzole | HCID 5070 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-(2-Chloroethyl)acetamide | HCID 81815 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline | HCID 3076411 | 21.1% |
Reaction Steps
2-Amino-6-trifluoromethoxybenzothiazole (9.4 g), N(2-chloroethyl)acetamide (9.7 g) and sodium iodide (13.5 g) in methyl ethyl ketone (30 cc) are heated for 40 hours to boiling. After cooling to a temperature in the region of 20° C., the reaction medium is added to distilled water (200 cc), treated with IN sodium hydroxide (40 cc) and then extracted with ethyl acetate (200 cc). After drying over magnesium sulphate and then concentration to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa), the residue is purified by chromatography on a silica column with a mixture of ethyl acetate and methanol (90:10 by volume) as eluent. 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline (2.7 g) is obtained, which product is converted to a hydrochloride subliming at about 180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05026717 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-834f28866e1046d99f9122dd971a08ff |
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| Source note | uspto-grants-1991_06 |
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