HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hept-2-yne → HCID 68583313, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hept-2-yne | HCID 14245 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | 5-{3-[2-(4-Bromo-benzyl)-4-(2,4-dichloro-phenyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxide | HCID 59305509 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68583313 | HCID 68583313 | — |
Reaction Steps
To a solution of 2-heptyne (129 μL, 1 mmol) in 2 mL dry THF at 0° C. was added 2 mL 0.5 M 9-BBN solution in THF. The resulting solution was stirred at room temperature under nitrogen for 4 hr. Then it was condensed under vacuum and used as boronic acid derivative according to general procedure G, reacting with 5-{3-[2-(4-bromo-benzyl)-4-(2,4-dichloro-phenyl)-imidazol-1-yl]-phenyl}-1,2,5-thiadiazolidine-3-one-1,1-dioxide (119 mg, 0.2 mmol) to give 5-(3-{4-(2,4-dichloro-phenyl)-2-[4-(1-methyl-hex-1-enyl)-benzyl]-imidazol-1-yl}-phenyl)-1,2,5-thiadiazolidine-3-one-1,1-dioxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404731B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-20a32e98f6684dda9716988eaf86ec27 |
| Source note | uspto-grants-2013_03 |