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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825733Generated: November 1, 2026

Tributylphosphine → HCID 69637133, compound

https://huagongshe.com/reaction/1825733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantN-PiperidinoethanolHCID 18232—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 69637194HCID 69637194—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69637133HCID 6963713322%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049312B1
Source datasetuspto-grants-2006_05
ORD IDord-4205e778472943009f0afe7f3c717565
Source noteuspto-grants-2006_05