Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 118271674 | HCID 118271674 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 73505440 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233979B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-7952c34faf6d4b0bab1af75a424d1891 |
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| Source note | uspto-grants-2016_01 |
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