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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273161Generated: October 29, 2026

HCID 67070560, compound → HCID 67070514, compound

https://huagongshe.com/reaction/273161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67070560HCID 67070560—
SolventFormic AcidHCID 284—
ProductHCID 67070514HCID 6707051497.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

(S)-[1-[3-(3-Chloro-phenyl)-[1,2,4]oxadiazol-5-yl]-2-(4-cyclopropyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-ethyl]-carbamic acid tert-butyl ester (135 mg) was mixed with 96% formic acid (1.3 mL) and heated at 50° C. for 1 h. The reaction mixture was concentrated in vacuo. The residue was quenched with saturated sodium bicarbonate and extracted with ethyl acetate. The organic layer was dried with sodium sulfate and concentrated. Purification was performed by flash column silica gel chromatography with 2-3% (2 M ammonia methanol) in dichloromethane to give 106 mg of the title compound as an off-white solid. 1H NMR (CDCl3): d ppm 8.73 (d, 2H), 8.03 (s, 1H), 7.93 (d, 1H), 7.69 (d, 2H), 7.46 (d, 1H), 7.42 (t, 1H), 5.02 (dd, 1H), 3.61 (dd, 1H), 3.49 (dd, 1H), 3.35 (m, 1H), 2.47 (br s, 2H), 1.20 (m, 2H), 0.75 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456200B2
Source datasetuspto-grants-2008_11
ORD IDord-b76ec2f6438d49a5b208301037f08516
Source noteuspto-grants-2008_11