HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86007768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | 4-Chloro-7-methoxyquinazolin-6-ol | HCID 23132475 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86007768 | HCID 86007768 | 76% |
Reaction Steps
Di-tert-butyl azodicarboxylate (1.44 g, 6.26 mmol) was added portionwise at room temperature to a stirred suspension of 4-chloro-7-methoxyquinazolin-6-ol (1.20 g, 5.70 mmol), 2-morpholin-4-ylethanol (0.82 g, 6.26 mmol) and triphenylphosphine (1.8 g, 6.87 mmol) in dichloromethane (25 ml). The reaction mixture was stirred for 2 hour and then the resulting orange solution was purified directly by silica gel chromatography eluting with a mixture of 3% methanol in dichloromethane and then purified further by chromatography on neutral alumina eluting with a 3% mixture of methanol in dichloromethane to give 4-chloro-7-methoxy-6-(2-morpholin-4-ylethoxy)quinazoline (1.40 g, 76% yield) as a pale yellow solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691867B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-2dfb9c434bfe45ae94f9edc4776731ef |
| Source note | uspto-grants-2010_04 |