HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonate → 4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonate | HCID 9954069 | — |
| Reactant | 3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chloride | HCID 86656208 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-one | HCID 66941775 | — |
Reaction Steps
3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chloride (13.2 g) and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate (21.7 g) dissolved in pyridine (500 mL) is stirred at room temperature for 7 d. Then, the pyridine is removed under reduced pressure and the residue is taken up in water (200 mL) and dichloromethane (200 mL). The organic phase is separated and the aqueous phase is extracted twice with dichloromethane. The combined organic phases are washed with 1 M hydrochloric acid, 1 M NaOH solution, and water. After drying (MgSO4), the solvent is evaporated under reduced pressure to yield the product as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859580B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-be2ab3346de140baa63765b2ac1f6b83 |
| Source note | uspto-grants-2014_10 |