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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467384Generated: October 31, 2026

Triphenylphosphine → HCID 56847526, compound

https://huagongshe.com/reaction/1467384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant5-ThiazolylmethanolHCID 2763216—
ReactantHCID 66611737HCID 66611737—
ReactantHCID 86689178HCID 86689178—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56847526HCID 56847526—

Reaction Steps

For the preparation, see also synthesis of 2-trimethylsilanylethyl {2-[1-(4-cyano-2-fluorophenyl)-7-methoxy-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-8-yloxy]-2-thiophen-2-ylethyl}carbamate under Example 3b: 3-fluoro-4-(8-hydroxy-7-methoxy-3-methyl-2-oxo-2,3-dihydroimidazo[4,5-c]quinolin-1-yl)benzonitrile (63 mg, 173 μmol), triphenylphosphine (polymer-bound) (294 mg, 1.12 mmol), thiazol-5-ylmethanol (62 mg, 540 μmol), diisopropyl azodicarboxylate (166 μl, 845 μmol) in tetrahydrofuran (7 ml) were reacted, giving 3-fluoro-4-[7-methoxy-3-methyl-2-oxo-8-(thiazol-5-ylmethoxy)-2,3-dihydroimidazo-[4,5-c]quinolin-1-yl]benzonitrile (15 mg, 32.5 μmol) as solid. MS: 462.0 (M+H+), TLC (HPTLC): Rf=0.44 (ethyl acetate/ethanol 2:1, parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000153B2
Source datasetuspto-grants-2015_04
ORD IDord-a606713949f147179f7eab8b168569f1
Source noteuspto-grants-2015_04