HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 22283108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 22283231 | HCID 22283231 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22283108 | HCID 22283108 | 18% |
Reaction Steps
N-(4-Benzyloxy-7-morpholin-4-yl-benzothiazol-2-yl)-4-chloromethyl-benzamide (1.0 g, 2.0 mmol) were dissolved in CH2Cl2 (10 ml) and treated at −78° C. with tetrabutyl ammonium iodide (0.95 g, 2.6 mmol) and a solution of boron trichloride in CH2Cl2 (1M, 7.4 ml). After subsequent warming to 0° and stirring for additional 2 h, ice (2 g) and then water (10 ml) and methanol (2 ml) were added and the phases separated. The aqueous phases were extracted twice with CH2Cl2/MeOH, the combined organic layers were dried with Na2SO4 and evaporated to dryness. Recrystallization from CH2Cl2/MeOH afforded the title compound as an off-white solid (18%). MS: m/e=403 ([M−H+]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317007B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-fc4b16a44be544d09f6aeda689adc3df |
| Source note | uspto-grants-2008_01 |