Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538996Generated: October 30, 2026

HCID 67033917, compound → HCID 178422941, compound

https://huagongshe.com/reaction/538996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67033917HCID 67033917—
ReactantHCID 67034104HCID 67034104—
ProductHCID 178422941HCID 17842294164%

Reaction Steps

(S)-4-isopropyl-3-(3-(3-methyl-4-(1H-1,2,4-triazol-3-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)oxazolidin-2-one (0.138 g, 64%) was prepared by the procedure described in Example 1, Step 9, using a mixture of (S)-4-isopropyl-3-(3-(3-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-3-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl) oxazolidin-2-one and (S)-4-isopropyl-3-(3-(3-methyl-4-(1-((2-(trimethylsilyl)ethoxy)methyl)-1H-1,2,4-triazol-5-yl)phenyl)pyrazolo[1,5-a]pyrimidin-5-yl)oxazolidin-2-one (0.285 g, 0.534 mmol), to produce a yellow solid. LCMS (APCI+) m/z 404.6 [M+H]+; 1H-NMR (400 MHz, CDCl3) δ 11.40 (broad s, 1H), 8.60 (d, J=7.8 Hz, 1H), 8.41 (s, 1H), 8.22 (s, 1H), 8.05 (d, J=7.8 Hz, 1H), 7.94 (s, 1H), 7.87 (d, J=8.0 Hz, 1H), 7.81 (d, J=8.2 Hz, 1H), 4.97-4.93 (m, 1H), 4.48-4.38 (m, 2H), 2.94-2.87 (m, 1H), 2.65 (s, 3H), 1.07 (d, J=7.0 Hz, 3H), 0.93 (d, J=6.8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865726B2
Source datasetuspto-grants-2014_10
ORD IDord-a263eb069c81454590ce7630830d012d
Source noteuspto-grants-2014_10