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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972961Generated: November 2, 2026

Dichloromethane → HCID 58529602, compound

https://huagongshe.com/reaction/1972961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant2-benzyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-IndazoleHCID 58529313—
ReactantHCID 58529650HCID 58529650—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventToluene ethanolHCID 21863594—
ProductHCID 58529602HCID 5852960257%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(4-Amino-5-bromo-pyrrolo[2,1-f][1,2,4]triazin-7-yl)-propan-1-ol (355 mg, 1.31 mmol) and 2-benzyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2H-indazole (656.4 mg, 1.96 mmol, 1.5 eq) were dissolved in 1:1 EtOH-toluene (11 mL each) and degassed with nitrogen. After 30 minutes [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complexed with dichloromethane (95.8 mg, 0.13 mmol, 0.1 eq) followed by 2M sodium carbonate solution (1.31 mL, 2.62 mmol, 2.0 eq) were added. The reaction mixture was stirred at 80° C. for 17 h and cooled to rt. The reaction mixture was partitioned between EtOAc and water and filtered through a pad of Celite® to rid of excess palladium salts. The organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified using an ISCO® instrument (gradient 1 to 100% [20% MeOH/DCM+1% Et3N]/DCM) and the product containing fractions were concentrated. Trituration with DCM-hexane gave 295.3 mg (57%) of the title compound as beige solid. 1H NMR (300 MHz, DMSO-d6) δ 8.54 (s, 1 H), 7.88 (s, 1 H), 7.80 (d, 1 H), 7.57 (s, 1 H), 7.34-7.28 (m, 5 H), 7.13 (dd, 1 H), 6.66 (s, 1 H), 5.65 (s, 2 H), 5.23 (d, 1H), 5.04 to 4.99 (m, 1H), 1.89 to 1.83 (m, 1H), 1.78 to 1.70 (m, 1H), 0.90 (t, 3H); ES-MS m/z 399.3 [M+H]+, RT (min) 2.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-ba22c10f151545ad887b8aabac381a7b
Source noteuspto-grants-2013_04