HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzo(B)Thiophene-2-Boronic Acid → HCID 20775778, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzo(B)Thiophene-2-Boronic Acid | HCID 2359 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 20775779 | HCID 20775779 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 20775778 | HCID 20775778 | 55.6% |
Reaction Steps
Suzuki coupling of 5-Bromo-3-(toluene-2-sulfonylamino)-thiophene-2-carboxylic acid tert-butyl ester (43 mg, 0.1 mmol) and benzothiophene-2-boronic acid (53.4 mg, 0.3 mmol) was carried out using Pd(PPh3)4 and Na2CO3 (as described in example 2) resulted in 5-Benzo[b]thiophen-2-yl-3-(toluene-2-sulfonylamino)-thiophene-2-carboxylic acid tert-butyl ester (27 mg, 55% yield). 1H NMR (CDCl3, 400 MHz) 9.92 (s, 1H), 8.07 (d, J=7.8 Hz, 1H), 7.79-7.71 (m, 2H), 7.45-7.24 (m, 7H), 2.7 (s, 3H), 1.56 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329924B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-48e9ba362b5c41d9b21b6ef52602c8ef |
| Source note | uspto-grants-2012_12 |