HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-Chloro-4-(3,4-dihydroisoquinolin-2(1h)-yl)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Product | 2-Chloro-4-(3,4-dihydroisoquinolin-2(1h)-yl)quinazoline | HCID 22692641 | — |
Reaction Steps
10 g Of the compound(50.2 mM) prepared in Preparation 2-1, 70 ml of dichloromethane and 7.8 ml of triethylamine (56 mM) were mixed and 6.4 ml of 1,2,3,4-tetrahydroisoquinoline(50.2 mM) was dropwise added slowly while maintaining the reaction temperature below 10° C., which was stirred at room temperature for 2 hours. The reaction mixture was dried over anhydrous sodium sulfate and concentrated under a reduced pressure. The residue was crystallized to give 14.6 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686458 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-2edcf17ed01c4c0ca1bb841cb09c39d3 |
| Source note | uspto-grants-1997_11 |