HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl chloroformate → Diphenyl (5-bromo-1,3-thiazol-2-yl)imidodicarbonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 5-Bromothiazol-2-amine monohydrobromide | HCID 2723848 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Diphenyl (5-bromo-1,3-thiazol-2-yl)imidodicarbonate | HCID 66858288 | 109.7% |
Reaction Steps
Phenyl chloroformate (1.4 ml, 11.0 mmol) was slowly added to a suspension of 5-bromo-thiazol-2-ylamine hydrobromide (1.3 g, 5.0 mmol) in 20 ml pyridine under an argon atmosphere. The reaction mixture was stirred for 3 h at room temperature and then concentrated under reduced pressure. The residue was suspended in water and acidified using conc. HCl to yield light brown crystals (2.3 g, 93%), m/e 419.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868030B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-3083999f38cb494792ba8586ba7b9a03 |
| Source note | uspto-grants-2011_01 |