HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Methyl-2-(5-(phthalimido)pentan-1-ylthio]-1,4,7b-triazacyclopent[cd]indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(5-Bromopentyl)phthalimide | HCID 136770 | — |
| Reactant | 1,2-Dihydro-3-methyl-1,4,7b-triazacyclopent[cd]inden-2-thione | HCID 135810293 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methyl-2-(5-(phthalimido)pentan-1-ylthio]-1,4,7b-triazacyclopent[cd]indene | HCID 21190203 | 79.5% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a suspension of 2.03 g (10.7 mmol) of 1,2-dihydro-3-methyl-1,4,7b-triazacyclopent[cd]inden-2-thione in 50 ml of N,N-dimethylformamide were added 3.18 g (10.7 mmol) of N-(5-bromopentyl)phthalimide and 2.24 ml (16.1 mmol) of triethylamine. The mixture was stirred for two hours at 100° C. After cooling, the resulting precipitates were collected by filtration, washed with N,N-dimethylformamide, ethanol, and diethylether, successively, dried to afford 3.44 g of the desired compound (79.3%, a pale brown solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251905B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-8ebc78c29e554ef2b3a6d6315e006581 |
| Source note | uspto-grants-2001_06 |