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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523967Generated: October 31, 2026

HCID 90313198, compound → HCID 90312381, compound

https://huagongshe.com/reaction/1523967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 90313198HCID 90313198—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 90312381HCID 9031238196.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 4′-(5-aminopyrazin-2-yl)-N-tert-butyl-2′,3′-difluorobiphenyl-2-sulfonamide (168 mg, 0.40 mmol) in TFA (3 mL) was heated at 50° Celsius for 3 hours. The reaction was then cooled to rt and carefully partitioned between NaHCO3 and EtOAc. The organic layer was isolated, dried over MgSO4, and concentrated to dryness. Purification by FCC afforded the title compound (140 mg, 96%). MS (ESI): mass calcd. for C16H12F2N4O2S, 362.06; m/z found, 363.1 [M+H]+. 1H NMR (500 MHz, DMSO-d6) δ 8.40 (s, 1H), 8.12-8.01 (m, 2H), 7.72-7.61 (m, 3H), 7.45-7.36 (m, 3H), 7.19 (m, 1H), 6.81 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079866B2
Source datasetuspto-grants-2015_07
ORD IDord-2983cd98e815420c8417378085672103
Source noteuspto-grants-2015_07