HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895896Generated: October 27, 2026
Propyl p-toluenesulfonate → Pramipexole p-toluenesulfonate
https://huagongshe.com/reaction/1895896
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propyl p-toluenesulfonate | HCID 69035 | — |
| Reactant | 2,6-Diamino-4,5,6,7-tetrahydrobenzothiazole | HCID 10329721 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | Pramipexole p-toluenesulfonate | HCID 86623293 | — |
Reaction Steps
Condition A: A 250 ml, three necked flask was equipped with a magnetic stirrer, a temperature probe, a heating mantle, a claisen joint, a reflux condenser, and a 100 ml addition funnel. The flask was charged with 5 grams of racemic 2,6 diamino-4,5,6,7-tetrahydro-benzothiazole, followed by 80 ml of n-propanol. Under continuous stirring, the mixture was heated to a temperature of 95° C. over 15 minutes generating a clear solution. The addition funnel was charged with a solution of 10.12 grams propyl tosylate and 8.2 ml diusopropylethyleamine in 28 ml n-propanol. This solution was added dropwise to the 250 ml flask with continuous stirring over a period of 2 hours. The reaction was continued with stirring for an additional 6 hours at 95° C., after which the solution was brought to room temperature, and stirring was continued for an additional 6 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518926B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-479d1cfe28db461a816fa6d8dfaade15 |
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| Source note | uspto-grants-2013_08 |
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