HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-(5-Chloro-1-isobutyl-indazol-7-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanesulfonic anhydride | HCID 81560 | — |
| Reactant | (5-Chloro-1-isobutyl-1H-indazole-7-yl)-methanol | HCID 118251601 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(5-Chloro-1-isobutyl-indazol-7-yl)acetonitrile | HCID 118251649 | — |
Reaction Steps
To a solution of compound 17 (1 g, 4.2 mmol), at room temperature and under nitrogen atmosphere, in dry dichloromethane (10 mL) were added DIPEA (0.8 mL, 4.62 mmol) and methane sulfonic anhydride. (0.8 g, 4.62 mmol) The resulting mixture was stirred for 2 h. Then, the reaction mixture was quenched with water and the mixture was extracted with more dichloromethane. The organic layer was separated, washed with Brine, dried (MgSO4), filtered and the solvent evaporated to give the desired product as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365569B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-7be3b221fdc040d19b85737e88ef271d |
| Source note | uspto-grants-2016_06 |