HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 5-[3-(1-pyrrolidinylmethyl)phenyl]-3-(1-{[3-(1-pyrrolidinyl)propyl]sulfonyl}-4-piperidinyl)-1H-indole-7-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(3-formylphenyl)-3-(1-{[3-(1-pyrrolidinyl)propyl]sulfonyl}-4-piperidinyl)-1H-indole-7-carboxamide | HCID 59003333 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 5-[3-(1-pyrrolidinylmethyl)phenyl]-3-(1-{[3-(1-pyrrolidinyl)propyl]sulfonyl}-4-piperidinyl)-1H-indole-7-carboxamide | HCID 59003311 | 8.1% |
Reaction Steps
To a solution of 5-(3-formylphenyl)-3-(1-{[3-(1-pyrrolidinyl)propyl]sulfonyl}-4-piperidinyl)-1H-indole-7-carboxamide (45.0 mg/0.086 mmol) in DCM/MeOH (1.0 ml/1.0 ml) was added pyrrolidine (0.043 mL, 0.517 mmol) and 1 drop of AcOH. The reaction mixture was stirred for 2 hr at r.t and then NaBH4 (17.0 mg, 0.086 mmol) was added. The reaction mixture was stirred for 30 min and concentrated and redissolved in 1.5 ml of DMSO. The residue was purified by using a Gilson semi-preparative HPLC system, eluting with 10% B to 80% B, where A=H2O (0.1% trifluoroacetic acid) and B=CH3CN (0.1% trifluoroacetic acid) pumped at 25 mL/min to give the title compound (4 mg, 8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858796B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-01d68fe41a6945008a9c91fe90b0d942 |
| Source note | uspto-grants-2010_12 |