HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 22139265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(Dimethylamino)-1-propanol | HCID 76646 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 7-hydroxy-2H-1,4-benzothiazin-3(4H)-one | HCID 820031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22139265 | HCID 22139265 | — |
Reaction Steps
N,N-dimethyl-3-aminopropanol (0.27 g, 5.2 mmol) was added to a mixture of 7-hydroxy-2H-1,4-benzothiazin-3(4H)-one (0.95 g, 5.2 mmol) and triphenylphosphine (1.37 g, 5.2 mmol) in dry tetrahydrofurane (30 ml) under nitrogen atmosphere, followed by diethyl azodicarboxylate (1 g, 5.7 mmol). The mixture was stirred at room temperature for 48 h, concentrated in vacuo, and the product was purified by silica gel chromatography using dichloromethane:methanol gradient of (9:1) to (7:3) as the mobile phase. Yield 1.1 g (75%) mp 120–121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07049312B1 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-7c01cc17f5624ac3b25c08fd54dc16e7 |
| Source note | uspto-grants-2006_05 |