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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535849Generated: October 29, 2026

N-Cyclobutyl-6-ethynylpyridazin-3-amine → HCID 72950081, compound

https://huagongshe.com/reaction/535849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Cyclobutyl-6-ethynylpyridazin-3-amineHCID 86709554—
Reactant4-chloro-3-iodo-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamideHCID 86709563—
ProductHCID 72950081HCID 72950081—

Reaction Steps

The title compound was synthesized from N-cyclobutyl-6-ethynylpyridazin-3-amine and 4-chloro-3-iodo-N-(4-(4-methyl-1H-imidazol-1-yl)-3-(trifluoromethyl)phenyl)benzamide in a manner similar to that described for in Example 1. The product was obtained as a pale yellow solid. Mp: 153-155° C.; 1H NMR (300 MHz, CDCl3) δ: 10.34 (1H, s), 8.36 (1H, s), 8.24-8.27 (1H, d, J=8.1 Hz), 8.03 (1H, s), 7.82-7.85 (1H, d, J=8.1 Hz), 7.48 (1H, s), 7.41-7.44 (1H, d, J=8.7 Hz), 7.34-7.37 (2H, t, J=9.3 and 8.7 Hz), 6.80 (1H, s), 6.61-6.64 (1H, d, J=9.6 Hz), 5.57-5.59 (1H, d, J=6.0 Hz), 4.22-4.29 (1H, m), 2.45-2.48 (2H, m), 2.28 (3H, s), 1.76-2.01 (4H, m). HRMS (ESI-TOF+): m/z [M+2H]+2 calcd for C28H24ClF3N6O: 276.0821. found: 276.0817.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859553B2
Source datasetuspto-grants-2014_10
ORD IDord-808d3e07603344b8ad9dd447a3857f40
Source noteuspto-grants-2014_10