HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 11533779, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide | HCID 59003280 | — |
| Product | HCID 11533779 | HCID 11533779 | 13% |
Reaction Steps
Following the general procedure for aminosulfonamide formation outlined in example 2, 3-{1-[(3-chloropropyl)sulfonyl]-4-piperidinyl}-5-phenyl-1H-indole-7-carboxamide (100 mg, 0.313 mmol) and N-(1-methylethyl)-2-propanamine (0.22 mL, 1.55 mmol) were allowed to react in the presence of K2CO3 (172.5 mg, 1.28 mmol). The resulting residue was purified by reverse phase HPLC eluting with 10% B to 80% B, where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% triflucaroacetic acid) to give the title compound (20.5 mg, 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858796B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-639c190e9718487e9936e7a11e60a875 |
| Source note | uspto-grants-2010_12 |