HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (S)-N-(1-{4-[1-(6-Chloro-2-pyrrolidin-1-yl-pyrimidin-4-yl)-piperidin-4-yl]-phenyl}-ethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4,6-Dichloro-2-(pyrrolidin-1-yl)pyrimidine | HCID 19353553 | — |
| Reactant | (S)-N-[1-(4-piperidin-4-yl-phenyl)ethyl]-acetamide | HCID 67125412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-N-(1-{4-[1-(6-Chloro-2-pyrrolidin-1-yl-pyrimidin-4-yl)-piperidin-4-yl]-phenyl}-ethyl)acetamide | HCID 86666705 | — |
Reaction Steps
To 22 mg (0.1 mmol) 4,6-dichloro-2-pyrrolidin-1-yl-pyrimidine in 1 mL THF are added 17 μL (0.1 mol) DIPEA and 25 mg (0.1 mmol) (S)—N-[1-(4-piperidin-4-yl-phenyl)ethyl]-acetamide (V.1). The mixture is stirred at rt over night. The solvent is removed in vacuo and the residue is purified using reversed phase HPLC (eluent A: water+0.1% TFA, eluent B: MeOH) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006450B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-d964d0db31ff41438675d8992344c6a7 |
| Source note | uspto-grants-2015_04 |