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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972972Generated: October 31, 2026

HCID 58529663, compound → HCID 58529448, compound

https://huagongshe.com/reaction/1972972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58529663HCID 58529663—
ReactantHCID 59231971HCID 59231971—
ProductHCID 58529448HCID 5852944890.8%

Reaction Steps

To the microwave vial was added tert-butyl 4-(4-amino-5-bromopyrrolo[2,1-f][1,2,4]triazin-7-yl)piperidine-1-carboxylate (250 mg, 0.63 mmol), 2-benzyl-5-fluoro-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2H-indazole (300 mg, 0.85 mmol, 1.35 eq), and tetrakis(trephenylphosphine)palladium (0) (46 mg, 0.063 mmol, 0.1 eq). Degassed, anhydrous DMF (6.3 mL) was added followed by 2.0M sodium carbonate solution (1.0 mL). The vial was capped and the reaction was irradiated in a microwave reactor at 180° C. for 25 min. The mixture was cooled to rt, diluted with EtOAc and filtered through a pad of Celite® to remove excess palladium. The filtrate was washed with 50% aqueous brine (3×), dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by ISCO® (gradient elution 0 to 10% MeOH/DCM) to give the product (309.7 mg, 68%) as an oil. 1H-NMR (300 MHz, CD3OD) 8.35 (s, 1H), 7.84 (s, 1H), 7.63 (d, 1H), 7.56 (d, 1H), 7.38 to 7.31 (m, 5H), 6.59 (s, 1H), 5.65 (s, 2H), 4.23 to 4.17 (m, 2H), 3.48 to 3.39 (m, 1H), 2.95 (broad s, 2H), 2.12 (d, 2H), 1.72 to 1.59 (m, 2H), 1.47 (s, 9H); ES-MS m/z 542.3 [M+H]+, RT (min) 3.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-ed89082edb364e0c8b5564d212e7b10f
Source noteuspto-grants-2013_04