HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-methoxycarbonyl-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chloro methylformate | HCID 12616564 | — |
| Reactant | 5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole | HCID 21295863 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-methoxycarbonyl-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole | HCID 19996494 | 6% |
Reaction Steps
Chloro methylformate (0.24 g, 0.0026 mol) dissolved in CH2Cl2 (5 ml) was added dropwise to a stirred solution of 5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole (0.80 g, 0.0022 mol) and triethylamine in CH2Cl2 (10 ml). The mixture was then stirred at room temperature for 19 h. The CH2Cl2 -solution was washed with water, dried (MgSO4) and the solvent was evaporated giving the desired product as an oil (0.06 g, 6%). NMR data for the final product is given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05039806 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-b0a0a202695f4d1ba74cd04fb694d5ff |
| Source note | uspto-grants-1991_08 |