HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68482452, compound → HCID 59443451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68482452 | HCID 68482452 | — |
| Reactant | HCID 68484099 | HCID 68484099 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 59443451 | HCID 59443451 | — |
Reaction Steps
The compound is prepared by the reaction of 3-bromo-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide (92.4 mg, 0.28 mmol, 1 eq) with 2-methoxy-6-(3-methoxyphenyl)naphthalene-1-ylboric acid (100 mg, 0.36 mmol, 1.3 eq) according to method C. The raw product was not characterized, but directly subjected to ether cleavage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546392B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-31d35bc05cec43c0b5c1ecabf8580793 |
| Source note | uspto-grants-2013_10 |