HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-(Benzoxazol-2-yl)-2-methyl-1-(3-(morpholin-4-yl)-n-propyl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethanimidic acid, methyl ester, hydrochloride (1:1) | HCID 10313100 | — |
| Reactant | 2-(N-(2-(morpholin-4-yl)-n-propyl)-2-nitroanilin-4-yl)benzoxazole | HCID 67498563 | — |
| Product | 5-(Benzoxazol-2-yl)-2-methyl-1-(3-(morpholin-4-yl)-n-propyl)benzimidazole | HCID 67498449 | 61% |
Reaction Steps
To a solution of 2-(2-(3-(morpholin-4-yl)-n-propyl)aminoanilin-4-yl)benzoxazole (see Working Example 96-1) (300 mg, 0.851 mmol) in methanol (5 mL) was added methyl acetimidate hydrochloride (103 mg, 0.936 mmol), and this was heated to reflux for 3 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, and this was extracted with ethyl acetate. After the organic layer obtained was dried over anhydrous sodium sulfate, it was filtered and concentrated. To the crystals obtained was added diethyl ether, this was filtered, washed with diethyl ether, and dried to yield the title compound (195 mg, 61% yield) as light brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-e4c8259744514d4c816fc342c2a97742 |
| Source note | uspto-grants-2014_09 |