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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870732Generated: October 31, 2026

Nitrogen → HCID 86696438, compound

https://huagongshe.com/reaction/870732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDichloromethaneHCID 6344—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
Reactant7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1-benzofuranHCID 43811027—
ReactantHCID 86696437HCID 86696437—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86696438HCID 86696438406.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a mixture of (3-bromo-imidazo[1,2-b]pyridazin-6-yl)-(4,4,4-trifluoro-butyl)-amine (442.4 mg, 1.4 mmol), 7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-2,3-dihydro-benzofuran [934586-50-2] (404.4 mg, 1.6 mmol), potassium phosphate tribasic monohydrate [27176-10-9] (632.1 mg, 2.7 mmol), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane [95464-05-4] (116.7 mg, 0.1 mmol) contained in a 50 mL round bottomed flask was added a solution of 30% (v/v) water in 1,2-dimethoxyethane (25 mL) and a magnetic stir bar. The reaction pot was fitted to a reflux condenser, lowered into an ambient temperature oil bath, and the system taken through 10 evacuation/N2 blanket cycles while being rapidly stirred. The rapidly stirred, N2 blanketed, reaction was heated to an oil bath temperature of 85° C. for 17 h then cooled and partitioned between brine (pH adjusted to 10 with 3N aqueous sodium hydroxide) and ethyl acetate. The phase separated extract was dried (MgSO4) and evaporated to afford brown solid which was purified by preparative RP-HPLC. Isolated product was dissolved in methanol, diluted with concentrated hydrochloric acid, evaporated to dryness, redissolved in methanol and precipitated by the addition of diethyl ether. Filtration of the precipitate yielded 162.0 mg of [3-(2,3-dihydro-benzofuran-7-yl)-imidazo[1,2-b]pyridazin-6-yl]-(4,4,4-trifluoro-butyl)-amine monohydrochloride salt as a white powder, mp. 299-300° C. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.88 (quin, J=7.52 Hz, 2H) 2.32-2.46 (m, 2H) 3.31 (t, J=8.84 Hz, 2H) 3.34-3.41 (m, 2H) 4.69 (t, J=8.72 Hz, 2H) 7.00 (t, J=7.71 Hz, 1H) 7.28 (d, J=9.85 Hz, 1H) 7.36 (dd, J=7.33, 1.01 Hz, 1H) 8.06 (d, J=9.85 Hz, 1H) 8.09 (br. s., 1H) 8.22 (d, J=8.08 Hz, 1H) 8.26 (s, 1H). 19F NMR (376 MHz, DMSO-d6) δ ppm −64.62. 13C NMR (100 MHz, DMSO-d6) δ ppm 20.40, 20.43, 29.04, 30.01, 30.29, 30.57, 30.84, 71.69, 108.63, 110.72, 118.75, 120.16, 121.07, 121.12, 123.71, 125.72, 125.99, 126.24, 128.07, 128.99, 132.10, 155.03, 156.77. LRMS (ESI) m/z 363.2 [(M+H)]+, calc'd for C18H17F3N4O: 362.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969565B2
Source datasetuspto-grants-2015_03
ORD IDord-a689d247fe98467e9d73685305de7684
Source noteuspto-grants-2015_03