HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-bromo-1-(5-bromo-2-methoxyphenyl)ethanone → HCID 25107258, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-bromo-1-(5-bromo-2-methoxyphenyl)ethanone | HCID 2756850 | — |
| Reactant | [3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]thiourea | HCID 71650841 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 25107258 | HCID 25107258 | 104% |
Reaction Steps
The title compound was prepared in analogy to example 1 step e) from 102 mg (0.33 mmol) 2-bromo-1-(5-bromo-2-methoxyphenyl)ethanone and 79 mg (0.3 mmol) [3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-thiourea. The crude reaction was diluted with diethyl ether and stirred for 15 minutes at room temperature. The product was filtered off and dried to yield 147 mg (99%) [4-(5-bromo-2-methoxy-phenyl)-thiazol-2-yl]-[3-methoxy-4-(4-methyl-imidazol-1-yl)-phenyl]-amine as a white solid. MS ISP (m/e): 472.8/470.9 (100/93) (M+H)+. 1H NMR (DMSO-D6, 250 MHz): δ (ppm)=10.74 (s, 1H), 9.30 (s, 1H), 8.34 (dd, 1H), 7.70 (s, 1H), 7.60 (s, 1H), 7.51 (d, 1H), 7.47 (d, 1H), 7.13 (d, 1H), 7.05 (d, 1H), 4.00 (s, 3H), 3.95 (s, 3H), 2.35 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910740B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-87a73dcdbfe840f1898c3d87b681a1ee |
| Source note | uspto-grants-2011_03 |