HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379991Generated: October 31, 2026
Dimethyl Sulfide → 5-Phenyl-1-(piperidin-4-yl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one
https://huagongshe.com/reaction/1379991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13450726 | HCID 13450726 | — |
| Product | 5-Phenyl-1-(piperidin-4-yl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one | HCID 13336285 | 90% |
Reaction Steps
A mixture of 100 mg (0.26 mmol) of the above product 12, 0.5 ml of methyl sulfide and 0.5 ml of methanesulfonic acid is heated at 70° C. for 5 hours. The reaction mixture is mixed with ice, basified with potassium carbonate and extracted with methylene chloride. The organic layer is washed with water, dried over anhydrous magnesium sulfate, and concentrated to give 73 mg of 1,3-dihydro-5-phenyl-1-(4-piperidinyl)-2H-1,4-benzodiazepin-2-one 13 as powders. The yield is 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04579685 |
|---|
| Source dataset | uspto-grants-1986_04 |
|---|
| ORD ID | ord-29212019790b4b73aec704143edc9a01 |
|---|
| Source note | uspto-grants-1986_04 |
|---|