HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 57991622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 57991648 | HCID 57991648 | — |
| Product | HCID 57991622 | HCID 57991622 | 43.6% |
Reaction Steps
A procedure similar to that in Example 7 was used. N-[5-n-butyl-4-(4-methoxy-phenyl)-thiazol-2-yl]-3,4-dimethoxy-benzamide prepared in Example 63 and boron tribromide were used as starting materials, the crude product was purified by recrystallization with acetone to give a product as a white solid in a yield of 43.6%, mp: 189-190 └. 1H-NMR (DMSO-d6, 400 MHz) δ: 0.88 (3H, t, J=7.2 Hz, CH3), 1.35 (2H, sextuple, J=7.20 Hz, CH2), 1.62 (2H, quintuple, J=7.20 Hz, CH2), 2.82 (2H, t, J=7.2 Hz, CH3), 6.07 (3H, br, OH), 7.65˜7.85 (3H, m, ArH), 7.32˜7.52 (4H, m, ArH), 12.12 (1H, br, CONH); EI-MS m/e (%): 384.1 (M+, 37), 248.2 (83), 205.1 (100); HREI-MS Calcd. for C20H20N2O4S: 384.1144. found: 384.1146.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053581B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-1d1150e6b1904cb786e1e0e4a46ef653 |
| Source note | uspto-grants-2011_11 |