Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630309Generated: November 1, 2026

Perchloric Acid → HCID 86691589, compound

https://huagongshe.com/reaction/1630309

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 86691589135.4%

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, 12.23 mmol) in CH2Cl2 (150 mL) and t-butyl acetate (105 mL) was added perchloric acid (3.15 mL, 36.7 mmol) at rt and sealed the reaction flask. After 3 h, the reaction mixture was diluted with CH2Cl2 (100 mL), carefully quenched with sat. NaHCO3 (50 mL), organic layer separated and washed with brine (100 mL), dried (Na2SO4), filtered and concentrated to give yellow liquid. This was purified by flash column chromatography on 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. 700 mg of starting material was also 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 numberUS08791108B2
Source datasetuspto-grants-2014_07
ORD IDord-059e92ba39a64dd1b4749c676a265e43
Source noteuspto-grants-2014_07