HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Propanesulfonyl chloride → 1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Propanesulfonyl chloride | HCID 66279 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Pyridin-2-ylazetidine-3-carbonitrile hydrochloride | HCID 68827153 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile | HCID 57798311 | — |
Reaction Steps
A suspension of 3-pyridin-2-ylazetidine-3-carbonitrile hydrochloride (365 mg, 1.9 mmol) in CH2Cl2 (10 mL) at 0° C. was treated with i-Pr2NEt (1.1 mL, 6.3 mmol) and n-PrSO2Cl (0.35 mL, 3.1 mmol) dropwise. After 4 h, the reaction was quenched with the addition of 2 M aqueous NaOH (10 mL) and stirred 72 h before being extracted with CH2Cl2 (3×20 mL). The combined organic extracts were dried (Na2SO4) and concentrated under reduced pressure to afford 1-(propylsulfonyl)-3-pyridin-2-ylazetidine-3-carbonitrile (II-1) as an orange oil. Analytical LCMS: single peak (214 nm), 2.664 min. This material was used in subsequent reactions without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572792B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-85be5606e24a4953b3d6be03293ed9a8 |
| Source note | uspto-grants-2009_08 |