HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220849Generated: October 29, 2026
4-(3,4-Dihydroxyphenyl)butyl amine hydrobromide → HCID 178479341, compound
https://huagongshe.com/reaction/2220849
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(3,4-Dihydroxyphenyl)butyl amine hydrobromide | HCID 11644630 | — |
| Reactant | methyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodide | HCID 140329753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178479341 | HCID 178479341 | 51% |
Reaction Steps
1-(3,5-Diamino-6-chloropyrazinoyl-2-methyl-pseudothiourea hydroiodide (0.2 g, 0.51 mmol) was added to a suspension of 27 in a mixture of THF (35 mL) and triethylamine (3 mL). The reaction mixture was stirred at reflux for 3 h, then the supernatant was separated and the solvent was removed under reduced pressure. The brown residue was washed with ether (2×30 mL) followed by addition of 10% HCl (5 mL). The solid material was collected, dissolved in methanol and precipitated by addition of ethyl acetate. The precipitate was washed with 10% HCl and dried to give compound 28 (131 mg, 51%) as a beige solid. 1H NMR (300 MHz, DMSO-d6) δ 1.52 (br s, 4H), 2.42 (m, 2H), 3.31 (m, 2H), 6.43 (m, 1H), 6.61 (m, 2H), 7.42 (br s, 2H), 7.90 (br s, 1H), 8.82 (br s, 1H), 8.98 (br s, 1H), 9.25 (s, 1H) 10.52 (s, 1H). APCI MS m/z=394 [C16H20ClN7O3+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368450B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-a6081ac8b2cf413ca8046ac48757e4b6 |
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| Source note | uspto-grants-2008_05 |
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