HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (5-Benzenesulfonyl-1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 69038045 | HCID 69038045 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-Benzenesulfonyl-1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester | HCID 69280061 | 95% |
Reaction Steps
To a solution of 0.087 g (1-methyl-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-carbamic acid tert-butyl ester in 1 ml of dichloromethane, 0.064 g of benzene sulfonyl chloride and 0.052 g of pyridine were added. The reaction mixture was stirred at room temperature for 16 hours. The reaction was quenched by addition of 1 M HCl (1 ml) and extracted with dichloromethane. The organic layer was washed with saturated NaHCO3, dried (MgSO4) and evaporated on the rotary evaporator to yield 0.113 g (95%) of the product as a light yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375099B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-4f71893ffc4e46a9b752612b58a526e6 |
| Source note | uspto-grants-2008_05 |