HuagongsheHuagongshe Chemistry Print Report · For research reference only
[4-(4-Aminobutyl)phenyl]acetic acid → HCID 178479335, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [4-(4-Aminobutyl)phenyl]acetic acid | HCID 22397301 | — |
| Reactant | methyl N-(3,5-diamino-6-chloropyrazine-2-carbonyl)carbamimidothioate;hydroiodide | HCID 140329753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178479335 | HCID 178479335 | 46.5% |
Reaction Steps
1-(3,5-Diamino-6-chloropyrazinoyl-2-methyl-pseudothiourea hydroiodide (0.2 g, 0.5 mmol) was added to a solution of 8 (0.7 g, 3.4 mmol) in THF (20 mL). The reaction mixture was stirred at reflux for 6 h, then the solvent was evaporated and the resultant oil was treated with 10% HCl (15 mL). The precipitate was isolated and crystallized twice from ethanol to give 9 (53 mg, 25%) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 1.59 (br s, 4H), 2.71 (m, 2H), 3.83 (s, 3H), 7.40 (d, 2H), 7.48 (br s, 2H), 7.80 (d, 2H), 8.92 (br s, 2H), 9.00 (br s, 1H), 9.48 (br s, 2H), 10.55 (s, 1H). APCI MS m/z=420 [C18H22ClN7O3+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189719B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-2573af35ca3746d5b485a35516a9f48b |
| Source note | uspto-grants-2007_03 |