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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504946Generated: October 25, 2026

Tributylphosphine → HCID 59136134, compound

https://huagongshe.com/reaction/504946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Reactant(R)-(-)-1-Methoxy-2-propanolHCID 2733589—
ReactantHCID 57476413HCID 57476413—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59136134HCID 5913613448%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N-{5-hydroxy-2-[5-(thiomorpholinomethyl)-4,5-dihydro-1,3-thiazol-2-yl]-1H-indol-7-yl}-N-methylpyridine-2-sulfonamide (145 mg) in toluene (2 mL) and tetrahydrofuran (1 mL) were added tributylphosphine (0.22 mL), (2R)-1-methoxypropan-2-ol (0.057 mL) and 1,1′-(azodicarbonyl)dipiperidine (220 mg), and the mixture was stirred at 80° C. for 3 hr, and concentrated. The residue was diluted with ethyl acetate, and subjected to basic silica gel column chromatography (eluate: ethyl acetate), and the obtained crude product was purified by silica gel column chromatography (hexane:ethyl acetate=3:1-1:2) to give the title compound (80 mg, yield 48%) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-c5b99814aca84820b45003ceb31fb7b1
Source noteuspto-grants-2010_08