HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86631460, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Indole-5-carboxaldehyde | HCID 589040 | — |
| Reactant | 4-(4-Methanesulfonyloxy-butyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 2784669 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86631460 | HCID 86631460 | — |
Reaction Steps
To a 0° C. solution of 1H-indole-5-carbaldehyde (0.43 g, 2.96 mmol) in DMF (10 mL) was added NaH (60% in mineral oil; 0.14 mg, 3.55 mmol). After 45 min at 0° C., a solution of 4-(4-methanesulfonyloxy-butyl)-piperidine-1-carboxylic acid tert-butyl ester (1.00 g, 3.15 mmol) in DMF (5 mL) was added dropwise. The mixture was warmed to rt and stirred for 18 h. The mixture was diluted with CHCl3 (20 mL) and washed with water (15 mL). The organic layer was dried and concentrated to obtain the crude residue, which was used purified by FCC to give 0.96 g (88%). MS: mass calcd. for C22H30N2O3, 370.23; m/z found, 371.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084466B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-955e79c016a3447fb3e350f9e5302160 |
| Source note | uspto-grants-2011_12 |