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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539024Generated: November 5, 2026

HCID 67033386, compound → HCID 178448161, compound

https://huagongshe.com/reaction/539024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67033386HCID 67033386—
ReactantHCID 67034254HCID 67034254—
ProductHCID 178448161HCID 17844816148%

Reaction Steps

(4S)-3-(3-(2-Fluoro-4-(1H-1,2,4-triazol-3-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-isopropyloxazolidin-2-one (0.186 g, 48%) was prepared by the procedure described in Example 1, Step 9, using a mixture of (4S)-3-(3-(2-fluoro-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-isopropyloxazolidin-2-one and (4S)-3-(3-(2-fluoro-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-5-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-isopropyloxazolidin-2-one (0.507 g, 0.943 mmol), to produce a yellow solid. LCMS (APCI+) m/z 408.6 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ 14.27 (broad s, 1H), 9.16 (d, J=7.8 Hz, 1H), 8.57-8.52 (m, 3H), 7.96-7.85 (m, 3H), 4.97-4.93 (m, 1H), 4.52-4.48 (m, 2H), 2.78-2.71 (m, 1H), 1.05 (d, J=7.1 Hz, 3H), 0.86 (d, J=6.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865726B2
Source datasetuspto-grants-2014_10
ORD IDord-34eb17a5481945d6a1f74fde6c77fbee
Source noteuspto-grants-2014_10