HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217934Generated: October 29, 2026
Diisopropylethylamine → HCID 178461613, compound
https://huagongshe.com/reaction/217934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67364433 | HCID 67364433 | — |
| Reactant | methyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodide | HCID 140329753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178461613 | HCID 178461613 | 73.4% |
Reaction Steps
1-(3,5-Diamino-6-chloropyrazinoyl-2-methylisothiourea hydriodide (0.39 g, 1.0 mmol) was added to a solution of 13 (0.49 g, 1.07 mmol) in THF (8 mL) containing diisopropylethylamine (0.18 mL, 2 mmol). The reaction mixture was stirred at reflux for 2.5 h and at room temperature overnight. After this time, the solvent was removed under reduced pressure. The brown residue was washed with ether (2×30 mL) and methylene chloride (2×10 mL). The residue was dissolved in a minimal volume of methanol (approx. 2 mL) and poured into water. The precipitate was collected, washed with water and dried overnight to give crude 11 (0.5 g) as a yellow solid. The compound II (0.4 g, 54%) was purified by flash chromatography on silica gel (eluent: chloroform/methanol/ammonium hydroxide=10:1:0.1) as a yellow solid. [α]D25=−20.4° (c=1.0, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198286B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-60f4e0c31c0548d78c45872a7b3aa608 |
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| Source note | uspto-grants-2012_06 |
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