HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719920Generated: October 30, 2026
Trifluoroacetic acid → 5-Methylsulfanylmethyl-pyrazin-2-ylamine
https://huagongshe.com/reaction/719920
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (5-Methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester | HCID 67482522 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonium Hydroxide | HCID 14923 | 0.1% |
| Product | 5-Methylsulfanylmethyl-pyrazin-2-ylamine | HCID 21897339 | 201.9% |
Reaction Steps
A solution of (5-methylsulfanylmethyl-pyrazin-2-yl)-carbamic acid tert-butyl ester (0.45 g, 1.762 mmol) in methylene chloride (18 mL) was treated with trifluoroacetic acid (1.4 mL, 18.172 mmol) and then was stirred at 25° C. for 2 h 15 min. The reaction solution was then treated with a second aliquot of trifluoroacetic acid (0.7 mL, 9.086 mmol) and was stirred at 25° C. for 5 h. At this time, the reaction mixture was concentrated in vacuo. Biotage chromatography (FLASH 40S, Silica, 1/9 methanol/methylene chloride with 0.1% ammonium hydroxide) afforded 5-methylsulfanylmethyl-pyrazin-2-ylamine (276.1 mg, quant.) as a white solid: mp 102.0–102.7° C.; EI-HRMS m/e calcd for C6H9N3S (M+) 155.0517, found 155.0516.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132425B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-4e9e437dc3bf4b389f8d3d4843900b0f |
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| Source note | uspto-grants-2006_11 |
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