HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2,4-Dimethoxyphenyl)butan-1-amine → HCID 178490100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2,4-Dimethoxyphenyl)butan-1-amine | HCID 22566135 | — |
| Reactant | methyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodide | HCID 140329753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178490100 | HCID 178490100 | 181.3% |
Reaction Steps
1-(3,5-Diamino-6-chloropyrazinoyl-2-methyl-pseudothiourea hydroiodide (0.3 g, 0.77 mmol) was added to an anhydrous THF solution (30 mL) of 79 (0.4 g, 1.9 mmol). The reaction mixture was stirred at reflux for 3 h then the solvent was evaporated. The residue was washed with ethyl acetate (2×20 mL) then treated with 3% HCl (15 mL). The yellow solid that formed was separated, washed with water and dried overnight to provide compound 80 (0.32 g, 90%). 1H NMR (300 MHz, DMSO-d6) δ1.57 (s, 4H), 2.50 (br s, 2H), 3.35 (br s, 2H), 3.73 (s, 3H), 3.76 (s, 3H), 6.43 (m, 1H), 6.52 (s, 1 H), 7.02 (m, 1H), 7.45 (br s, 2H), 8.86 (br s, 1H), 8.99 (br s, 1H), 9.03 (m, 1H), 10.56 (s, 1H). APCI MS m/z 422 [C18H24ClN7O3+H]r+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858614B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-f68c3ab3fb28413c97acb3a2e5dd6ef0 |
| Source note | uspto-grants-2005_02 |