HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dimethoxybenzylamine → HCID 25052214, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | HCID 58055059 | HCID 58055059 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25052214 | HCID 25052214 | — |
Reaction Steps
1-(3,4-dichlorobenzyl)-3-(4-(iodomethyl)thiazol-2-yl)urea (Intermediate XXII) was taken up in THF and an excess of the 2,4-dimethoxy-benzylamine (20 equiv.) was added. The reaction was allowed to stir overnight at room temperature. The volatiles were removed in vacuo. Resulting oil triturated with water to give a gooey solid. Water was decanted off and resulting residue was purified by column chromatography (DCM, 0-8% MeOH saturated with NH3). 1H NMR (400 MHz, CDCl3): 7.32 (d, 1H), 7.19 (br s, 1H), 7.01 (br d, 1H), 6.96 (d, 1H), 6.60 (s, 1H), 6.40-6.33 (m, 2H), 4.11 (br s, 2H), 3.78 (s, 3H), 3.71 (s, 3H), 3.69 (br s, 2H), 3.55 (br s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716320B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-1ecfbbe89cc843b38ef2fbdcbc69cc91 |
| Source note | uspto-grants-2014_05 |