HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523967Generated: October 31, 2026
HCID 90313198, compound → HCID 90312381, compound
https://huagongshe.com/reaction/1523967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 90313198 | HCID 90313198 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 90312381 | HCID 90312381 | 96.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079866B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-2983cd98e815420c8417378085672103 |
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| Source note | uspto-grants-2015_07 |
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