HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzothiazolamine, 6-bromo- → 6-(4-(Benzyloxy)-3-fluorophenyl)benzo[d]thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzothiazolamine, 6-bromo- | HCID 85149 | — |
| Reactant | 4-Benzyloxy-3-fluorophenylboronic Acid | HCID 2737788 | — |
| Product | 6-(4-(Benzyloxy)-3-fluorophenyl)benzo[d]thiazol-2-amine | HCID 59283013 | — |
Reaction Steps
Compound 6-(4-(benzyloxy)-3-fluorophenyl)benzo[d]thiazol-2-amine (W146) was prepared using the general procedure for Suzuki coupling reaction between 4-(benzyloxy)-3-fluorophenylboronic acid (100 mg, 0.4 mmol) and 6-bromobenzo[d]thiazol-2-amine (92 mg, 0.4 mmol), as a white solid (65 mg, 58%). 1H NMR (400 MHz, acetone-d6) δ 7.92 (d, J=2.0 Hz, 1 H), 7.54-7.51 (m, 3 H), 7.49-7.46 (m, 1 H), 7.46-7.40 (m, 4 H), 7.37-7.33 (m, 1 H), 7.30-7.26 (m, 1 H), 6.86 (brs, 2 H), 5.25 (s, 2 H); MS (ESI) m/z 351 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420052B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-ab737ae43b8a4104a9adea0a85353317 |
| Source note | uspto-grants-2013_04 |