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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590852Generated: October 30, 2026

Triethylsilane → HCID 73505440, compound

https://huagongshe.com/reaction/590852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 118271674HCID 118271674—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 73505440HCID 73505440—

Reaction Steps

(R)-1-(3-isopropyl-1-trityl-1,3,4,5-tetrahydropyrazolo[3,4,5-de][1,6]naphthyridin-7-yl)-3-(1-phenylethyl)urea (75 mg, 0.123 mmol) was taken in TFA (0.5 mL) and stirred at room temperature for 30 minutes before triethylsilane (155 uL, 0.97 mmol) was added. The reaction mixture was stirred for 15 minutes at room temperature then heated at 80° C. for 30 minutes before it was concentrated, taken in DCM and washed with aqueous sodium bicarbonate, brine, dried with sodium sulfate and concentrated. Purification of the residue by flash column (0-15% MeOH-DCM) gave (R)-1-(3-isopropyl-1,3,4,5-tetrahydropyrazolo[3,4,5-de][1,6]naphthyridin-7-yl)-3-(1-phenylethyl)urea. MS ESI calc'd. for C20H24N6O [M+H]+ 365. found 365. 1H NMR (ppm, 500 MHz, DMSO-d6) δ 7.34-7.23 (m, 4H), 7.18 (m, 1H), 6.40 (s, 1H), 4.90 (m, 1H), 3.40 (m, 2H), 3.22 (m, 2H), 2.90 (m, 1H), 1.38 (d, J=7.0, 3H), 1.07 (d, J=9.4, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-7952c34faf6d4b0bab1af75a424d1891
Source noteuspto-grants-2016_01