Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468745Generated: November 3, 2026

Perchloric Acid → HCID 86691589, compound

https://huagongshe.com/reaction/1468745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerchloric AcidHCID 24247—
Reactant(S)-ethyl 6-(2-ethoxy-1-hydroxy-2-oxoethyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylateHCID 86691588—
SolventDichloromethaneHCID 6344—
Solventtert-Butyl acetateHCID 10908—
ProductHCID 86691589HCID 86691589135.7%

Reaction Steps

To a stirred solution of (S)-ethyl 6-(2-ethoxy-1-hydroxy-2-oxoethyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate (5.3 g, 12.2 mmol) in CH2Cl2 (150 mL) and t-butyl acetate (105 mL) at rt was added perchloric acid (3.15 mL, 36.7 mmol). The reaction flask was sealed. After stirring for 3 h, the reaction mixture was diluted with CH2Cl2 (100 mL), carefully quenched with sat. aq. NaHCO3 (50 mL). The organic layer was separated and washed with brine (100 mL), dried (Na2SO4), filtered and concentrated in vacuo to give a yellow liquid. This crude product was purified by flash column chromatography on a silica gel column using (10-50% EtOAc/Hex as eluant) to afford the desired (S)-ethyl 6-(1-(tert-butoxy)-2-ethoxy-2-oxoethyl)-7-iodo-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate (4.5 g, 8.28 mmol, 67.7% yield) as viscous oil. In addition, 700 mg of starting material was recovered. 1H NMR (500 MHz, CDCl3) δ 7.31 (s, 1H), 5.56 (s, 1H), 4.51 (q, J=7.1 Hz, 2H), 4.26-4.16 (m, 2H), 2.71 (s, 3H), 1.48 (t, J=7.2 Hz, 3H), 1.30 (s, 9H), 1.23 (t, J=7.0 Hz, 3H). LCMS (M+H)=490.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006235B2
Source datasetuspto-grants-2015_04
ORD IDord-fb900eccbc784f61b910508352204d38
Source noteuspto-grants-2015_04