HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11393673, compound → HCID 18183133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11393673 | HCID 11393673 | — |
| Reactant | HCID 18183154 | HCID 18183154 | — |
| Catalyst | Mercuric oxide | HCID 30856 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 18183133 | HCID 18183133 | — |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
A suspension of 0.50 g (1.47 mmol) of 5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-8-thione (Example 15D) and 0.42 g (2.94 mmol) of 2-aminomethyl-2-cyclopropyl-1,3-dioxolane in 12 ml of Methyl Cellosolve® with 0.32 g (1.47 mmol) of red mercury oxide is stirred for 12 hours at 110° C. After filtration, the mixture is concentrated by evaporation to a volume of 5 ml and poured into water. The precipitate is suctioned off and dissolved in 10 ml of a 1:1 mixture of concentrated hydrochloric acid and glacial acetic acid and heated to boiling for 1.5 hours. During cooling, the hydrochloride salt of the title compound precipitates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06600036B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-2a4f83610b304b8baf94e34c7a061827 |
| Source note | uspto-grants-2003_07 |