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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472835Generated: October 30, 2026

tert-Butyl acetate → HCID 86670278, compound

https://huagongshe.com/reaction/472835

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantPerchloric AcidHCID 24247—
Reactant(S)-methyl 2-(7-chloro-2-(3-chlorophenyl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetateHCID 86670276—
SolventDichloromethaneHCID 6344—
ProductHCID 86670278HCID 8667027850%

Reaction Steps

To a solution of (S)-methyl 2-(7-chloro-2-(3-chlorophenyl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)-2-hydroxyacetate (1.0 g, 2.73 mmol) in CH2Cl2 (100 mL) at room temperature was added tert-butyl acetate (20 mL) followed by perchloric acid (0.282 mL, 3.28 mmol). The reaction mixture was stirred for 16 h at room temperature. The reaction mixture was quenched with water and diluted with ethyl acetate. The organic phase was washed with saturated NaHCO3 and dried over sodium sulfate. The solvent was evaporated. Purification by silica gel chromatography provided the title compound (520 mg, 50%). 1H NMR (400 MHz, CHLOROFORM-d) δ 8.07-8.00 (m, 1H), 7.89 (dt, J=6.7, 1.9 Hz, 1H), 7.48-7.37 (m, 2H), 6.93 (s, 1H), 5.68 (s, 1H), 3.75 (s, 3H), 2.69 (s, 3H), 1.29 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633200B2
Source datasetuspto-grants-2014_01
ORD IDord-6024ceb0540a42dcabffff8da0687811
Source noteuspto-grants-2014_01