HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid cyanomethyl-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| Reactant | 3-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid | HCID 66918698 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2-Chloro-benzenesulfonyl)-cyclopentanecarboxylic acid cyanomethyl-amide | HCID 72340426 | — |
Reaction Steps
A solution of 3-(2-chloro-benzenesulfonyl)-cyclopentanecarboxylic acid (0.25 g, 1.0 eq) in DMF (4.0 mL) was treated with DIPEA (0.22 mL, 1.5 eq) and HATU (0.39 g, 1.2 eq). The mixture was stirred at RT for 15 min, then a solution of aminoacetonitrile hydrochloride (0.12 g, 1.5 eq) and DIPEA (0.22 mL, 1.5 eq) in DMF (1 mL) was added. The resulting solution was stirred at RT overnight and then purified by preparative HPLC. The title compound was obtained as a light yellow gum (0.10 g, 37%). MS (ESI): m/z=327.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893099B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-6eae7c787ec64b32a25c88b4589546f0 |
| Source note | uspto-grants-2011_02 |