HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-((3-(3-Methylfuran-2-carboxamido)phenyl)ethynyl)nicotinic acid → N-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl](methyl)oxido--sulfanylidene}-5-({3-[(3-methyl-2-furoyl)amino]phenyl}-ethynyl)nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-((3-(3-Methylfuran-2-carboxamido)phenyl)ethynyl)nicotinic acid | HCID 57657847 | — |
| Reactant | tert-Butyl(dimethyl) {[4-(S-methylsulfonimidoyl)benzyl]oxy}silane | HCID 57657970 | — |
| Product | N-{[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl](methyl)oxido--sulfanylidene}-5-({3-[(3-methyl-2-furoyl)amino]phenyl}-ethynyl)nicotinamide | HCID 57657965 | 71% |
Reaction Steps
In a manner similar to that described in Example 480 (step 6), tert-Butyl(dimethyl) {[4-(S-methylsulfonimidoyl)benzyl]oxy}silane (0.485 g, 1.62 mmol) and 5-((3-(3-methylfuran-2-carboxamido)phenyl)ethynyl)nicotinic acid (0.561 g, 1.62 mmol) were reacted to give the title compound (0.722 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915443B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-8d1014934ece46a387e590707d91383f |
| Source note | uspto-grants-2011_03 |