HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(6-Methoxy-quinazolin-4-yloxymethyl)-cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | L-Pyroglutamic Acid | HCID 7405 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(6-Methoxy-quinazolin-4-yloxymethyl)-cyclohexanol | HCID 21104630 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(6-Methoxy-quinazolin-4-yloxymethyl)-cyclohexanone | HCID 21104631 | — |
Reaction Steps
Triethylamine (10 ml, 71 mmol) and then, in portions, Pyr.SO3 (5.8 g, 36 mmol), were added at 0° C. to a solution of 4-(6-methoxy-quinazolin-4-yloxymethyl)-cyclohexanol (2.88 g, 10 mmol) in DMSO (30 ml). The reaction mixture was stirred at that temperature for 15 minutes and then allowed to come to room temperature. After 2 hours, water (300 ml) was added. The aqueous phase was extracted with ether (3×150 ml). The combined organic phases were washed with saturated sodium chloride solution, dried over MgSO4 and concentrated. The crude product was purified by chromatography on silica gel (EtOAc/hex 1/2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223776B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-345c55533fd44f4f9ffd94a869e5a555 |
| Source note | uspto-grants-2007_05 |