HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 66916321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 21956426 | HCID 21956426 | — |
| Reactant | HCID 135545160 | HCID 135545160 | — |
| Product | HCID 22260370 | HCID 22260370 | — |
| Product | HCID 66916321 | HCID 66916321 | 40% |
Reaction Steps
To the DMF solution (10 mL) of tert-butyl 4-(7-hydroxy-6-methoxyquinazolin-4-yl)piperazinecarboxylate (1.88 g, 5 mmol), Cs2CO3 (3.3 g, 10 mmol) added 1-chloroethyl-tosylate (1.8 mL, 10 mmol). The mixture was stirred overnight at room temperature. The solvent was evaporated and the crude residue was purified by RP-HPLC to afford the intermediate tert-butyl-4-[6-methoxy-7-(2-chloroethoxy)quinazolin-4-yl]piperazinecarboxylate as the desired product (850 mg, 40%). MS(ES) 423 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329655B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-0054219531f04ba0901ed4bc9d6a8595 |
| Source note | uspto-grants-2008_02 |