HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrile → HCID 86592939, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrile | HCID 16090854 | — |
| Reactant | HCID 64538625 | HCID 64538625 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86592939 | HCID 86592939 | — |
Reaction Steps
To a stirred solution of (2S,5R)-1-(chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrile (0.05 g, 0.25 mmol, Example 8D) in acetonitrile (3 mL ) at room temperature under nitrogen, was added 6-(2-amino-2-methyl-propoxy)-nicotinonitrile (0.1 g, 0.508 mmol). The reaction mixture was stirred overnight and then concentrated under reduced pressure. The residue was flash chromatographed with 2% MeOH/CH2Cl2 to provide the desired compound as a white solid. MS (DCI) m/z 352 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 2.01-2.04 (2H, m), 2.05 (2H, s), 2.07 (2H, s), 3.03 (1H, m), 3.04 (6H, s), 3.5-4.57 (2H, m), 4.57-4.58 (1H, m), 4.58-5.59 (1H, m), 7.0-7.08 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238724B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-ed511a3dad664ea9a84dd61c79b281aa |
| Source note | uspto-grants-2007_07 |