HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Biphenyl-4-yl-boronic acid → Methyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Biphenyl-4-yl-boronic acid | HCID 151253 | — |
| Reactant | Methyl 5-methylthio-4-[(4-phenylphenyl)amino]thiophene-2-carboxylate | HCID 18537271 | — |
| Reactant | Methyl 4-amino-5-methylthiothiophene-2-carboxylate | HCID 86583856 | — |
| Product | Methyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate | HCID 86583857 | 19.1% |
Reaction Steps
Methyl 5-methylthio-4-[(4-phenylphenyl)amino]thiophene-2-carboxylate: Using a procedure similar to Example 208, step (a), 74.4 mg (0.36 mmol) of methyl 4-amino-5-methylthiothiophene-2-carboxylate was allowed to react with 142.5 mg (2 equiv, 0.72 mmol) of 4-phenylphenyl boronic acid to give 24.5 mg (19.1%) of methyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate. 1H NMR (CDCl3, 400 MHz) δ 2.45 (s, 3H), 3.92 (s, 3H), 6.38 (bs, 1H), 7.08-7.14 (m, 2H), 7.33 (m, 1H), 7.43-7.46 (m, 2H), 7.54-7.60 (m, 411), 7.82 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562840B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-ebd3e7c961764c3cb1b5805f9db4e89d |
| Source note | uspto-grants-2003_05 |