HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl isocyanate → N1-(N'-phenylcarbamoyl)-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole | HCID 21295863 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N1-(N'-phenylcarbamoyl)-5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole | HCID 53654244 | 5% |
Reaction Steps
Phenylisocyanate (0.20 g, 0.00167 mol) dissolved in CH2Cl2 (5 ml) was added dropwise under stirring to a solution of 5,6-methylenedioxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole (0.50 g, 0.00139 mol) and triethylamine (0.28 g, 0.00278 mol) in CH2CL2 (15 ml). The mixture was then stirred at room temperature for 50 hours. The CH2Cl2 -solution was washed with water, dried (MgSO4) and the solvent was evaporated giving the desired product as an oil (0.03 g, 5%). 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-9c2e9a64e5fa4f8aa1a4e807c172b390 |
| Source note | uspto-grants-1991_08 |