HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Bis(benzyloxycarbonyl)-2-methylisothiourea → HCID 178432740, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Bis(benzyloxycarbonyl)-2-methylisothiourea | HCID 4664213 | — |
| Reactant | Tert-butyl [3-(5-amino-6-methylpyridin-3-yl)propyl]carbamate | HCID 68222687 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178432740 | HCID 178432740 | 61% |
Reaction Steps
To a solution of tert-butyl[3-(5-amino-6-methylpyridin-3-yl)propyl]carbamate (2.99 g, 11.3 mmol), 1,3,-bis(benzyloxycarbonyl)-2-methyl-2-thiopseudourea (3.41 g, 9.51 mmol), and mercury(II)chloride (3.37 g, 12.4 mmol) in DCM (100 mL) was added TEA (5.19 mL, 37.3 mmol) dropwise via syringe. The reaction mixture was allowed to stir at rt overnight. The reaction mixture was filtered over a pad of Celite® and the resulting filtrate was concentrated. The residue was purified by column chromatography to give dibenzyl{(Z)-[(5-{3-[(tert-butoxycarbonyl)amino]propyl}-2-methylpyridin-3-yl)amino]methylylidene}biscarbamate (3.34 g, 61%) as a white solid. LCMS (FA): Rt=1.90 min, m/z=576.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998952B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-f1f72c155c4f435db249f828aeeae347 |
| Source note | uspto-grants-2011_08 |