HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylphosphine → HCID 69637133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | N-Piperidinoethanol | HCID 18232 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | HCID 69637194 | HCID 69637194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69637133 | HCID 69637133 | 22% |
Reaction Steps
To a solution of (Z)-2[(5-hydroxyindol-3-yl)methylene]-2H-1,4-benzothiazin-3(4H)-one (1.00 g, 3.24 mmol) and 1,1′-(azodicarbonyl)dipiperidine (1.23 g, 4.87 mmol) in dry tetrahydrofurane-(40 ml), tributylphosphine (0.98 g, 4.87 mmol) was added under nitrogen atmosphere keeping the mixture at 0–5° C. After 5 min N-(2-hydroxyethyl)piperidine (0.63 g, 4.88 mmol) was added at the same temperature. The cooling bath was removed and the mixture stirred at room temperature for 48 h. Then the solvent was removed under reduced pressure and the residue chromatographed (silica gel, eluent, ethyl acetate:ethanol (90:10) to (80:20)) to yield 0.2 g (22%) of the entitled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07049312B1 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-4205e778472943009f0afe7f3c717565 |
| Source note | uspto-grants-2006_05 |