HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-DI-Boc-2-methylisothiourea → HCID 178432665, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-DI-Boc-2-methylisothiourea | HCID 546603 | — |
| Reactant | HCID 59405032 | HCID 59405032 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178432665 | HCID 178432665 | 48% |
Reaction Steps
To a solution of 2-methyl-5-(1,3,3-trimethylpiperidin-4-yl)pyridine-3-amine (0.814 g, 3.49 mmol) in DCM (50 mL) were added 1,3-bis(tert-butoxycarbonyl)-2-methyl-2-thiopseudourea (1.52 g, 5.23 mmol), mercury (II) chloride (1.42 g, 5.23 mmol) and TEA (2.92 mL, 20.9 mmol). The reaction mixture was allowed to stir overnight at rt then filtered through a Celite® pad and washed with DCM. The filtrate was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to give di-tert-butyl((Z)-{[2-methyl-5-(1,3,3-trimethylpiperidin-4-yl)pyridine-3-yl]amino}methylylidene)biscarbamate (0.79 g, 48%) as a white solid. LCMS (FAL): Rt=5.08 min, m/z=476.6 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507667B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-bc0b929de7db4eb9a44a691569899221 |
| Source note | uspto-grants-2013_08 |