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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539022Generated: November 3, 2026

HCID 67033445, compound → HCID 178448160, compound

https://huagongshe.com/reaction/539022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67033445HCID 67033445—
ReactantHCID 67033567HCID 67033567—
ProductHCID 178448160HCID 17844816065%

Reaction Steps

(4S)-3-(3-(2-Chloro-4-(1H-1,2,4-triazol-3-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-isopropyloxazolidin-2-one (0.078 g, 65%) was prepared by the procedure described in Example 1, Step 9, using a mixture of (4S)-3-(3-(2-chloro-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-chloro-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 (0.158 g, 0.285 mmol), to produce a yellow solid. LCMS (APCI+) m/z 424.6 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ 14.21 (broad s, 1H), 9.13 (d, J=7.8 Hz, 1H), 8.64 (s, 1H), 8.29 (s, 1H), 8.15 (s, 1H), 8.08 (m, 1H), 8.00 (d×d, J=8.2, 1.5 Hz, 1H), 7.93 (d, J=7.8 Hz, 1H), 4.85-4.81 (m, 1H), 4.45-4.44 (m, 2H), 2.70-2.66 (m, 1H), 0.95 (d, J=7.1 Hz, 3H), 0.84 (d, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865726B2
Source datasetuspto-grants-2014_10
ORD IDord-f3a86b25a1c04814a47b8a6215ba2976
Source noteuspto-grants-2014_10