HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 68881362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | 5-Chloro-7-(3-methoxyprop-1-ynyl)-1,3-benzodioxol-4-amine | HCID 21082716 | — |
| Reactant | 4-Chloro-7-(2-chloroethoxy)-6-methoxyquinazoline | HCID 59682907 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68881362 | HCID 68881362 | — |
Reaction Steps
A solution of sodium bis(trimethylsilyl)amide (5.6 ml) in tetrahydrofuran (1.0M, 5.6 mmol) was added dropwise to an ice-cold solution of 4-chloro-7-(2-chloroethoxy)-6-methoxyquinazoline (0.7 g, 2.6 mmol) and 5-chloro-7-(3-methoxyprop-1-yn-1-yl)-1,3-benzodioxol-4-amine (0.675 g, 2.8 mmol) in dimethylformamide (8 ml). The mixture was allowed to warm to room temperature over 3 hours. A saturated solution of ammonium chloride was added and the mixture was partitioned between water and dichloromethane. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure. Flash chromatography on silica eluting with a mixture of 30-100% ethyl acetate in hexane gave the product as a solid. (0.608 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504408B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-c68572d711c844ab8834df9b2d660fa7 |
| Source note | uspto-grants-2009_03 |