Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025601Generated: October 31, 2026

Tetrahydrofuran → HCID 86673716, compound

https://huagongshe.com/reaction/1025601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 86673717HCID 86673717—
SolventWaterHCID 962—
ProductHCID 86673716HCID 86673716—

Reaction Steps

1-[3-(6-tert-Butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-2-formyl-phenyl]-3-[4-(1-hydroxy-1-methyl-ethyl)-phenylamino]-1H-pyrazole-4-carbonitrile (78 mg, 0.14 mmol) and dihydrogen tris(dimethylphosphinito)hydroplatinate (7.1 mg, 0.12 eq) were taken up in tetrahydrofuran (3.1 ml) and water (0.31 ml). The material was stirred and heated to reflux (oil bath) for 1 hour. The mixture was cooled to ambient and the volatiles were stripped (rotary evaporator). The crude material was purified by preparative thin layer chromatography (2 plates, eluting first with 7% methanol in methylene chloride and then re-developing with 6% methanol in methylene chloride). The product band was collected, providing desired 1-[3-(6-tert-butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-2-formyl-phenyl]-3-[4-(1-hydroxy-1-methyl-ethyl)-phenylamino]-1H-pyrazole-4-carboxylic acid amide as a light yellow powder (41 mg). LC/MS calcd for C32H31FN6O4 (m/e) 582.62, obsd 581.0 (M−H, ES−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729078B2
Source datasetuspto-grants-2014_05
ORD IDord-80c54ab875184a07a0e4d9a837f6f633
Source noteuspto-grants-2014_05