HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoyl isothiocyanate → N-((7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-yl)carbamothioyl)-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoyl isothiocyanate | HCID 141398 | — |
| Reactant | HCID 77230928 | HCID 77230928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-((7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-yl)carbamothioyl)-4-nitrobenzamide | HCID 86658374 | 112.7% |
Reaction Steps
A reaction mixture of 2-(5-amino-7-bromo-3-chloro-5H-chromeno[2,3-c]pyridin-5-yl)ethanol (2.8 g, 7.87 mmol) and 4-nitrobenzoyl isothiocyanate (1.639 g, 7.87 mmol) in THF (100 mL) was stirred at RT for 1 hour. The reaction mixture was then concentrated under reduced pressure to afford N-(7-bromo-3-chloro-5-(2-hydroxyethyl)-5H-chromeno[2,3-c]pyridin-5-ylcarbamothioyl)-4-nitrobenzamide (5 g, 8.87 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497264B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-6c96b966570c49558be70a157c04a85f |
| Source note | uspto-grants-2013_07 |