HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → [2-(1-Amino-cyclopropyl)-pyridin-4-ylmethyl]-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-[(tert-Butoxycarbonylamino)methyl]-2-cyanopyridine | HCID 23298149 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(1-Amino-cyclopropyl)-pyridin-4-ylmethyl]-carbamic acid tert-butyl ester | HCID 67390399 | — |
Reaction Steps
To a solution of (2-cyano-pyridin-4-ylmethyl)-carbamic acid tert-butyl ester (1.2 g, 5.1 mmol) in THF (100 mL) was added ethylmagnesium bromide (3 M, 3.3 mL, 10 mmol) and titanium isopropoxide (2.3 mL, 7.7 mmol). The reaction mixture was stirred at room temperature for 16 h. Water was added (5 mL) and the resulting solids filtered off. The organics were concentrated, then purified by flash chromatography on silica gel using 5-10% MeOH/CH2Cl2 to afford [2-(1-amino-cyclopropyl)-pyridin-4-ylmethyl]-carbamic acid tert-butyl ester as a solid, m/z 264.4 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552205B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-1c583627cf7048e5bf7e3b896e4ee8c1 |
| Source note | uspto-grants-2013_10 |