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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972977Generated: October 31, 2026

Sodium Carbonate → HCID 69303364, compound

https://huagongshe.com/reaction/1972977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
ReactantHCID 69328881HCID 69328881—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 69303364HCID 6930336469.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of 4-amino-7-bromopyrrolo[2,1-f][1,2,4]triazine-6-carbonitrile (1.00 g, 4.20 mmol) and tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydropyridine-1(2H)-carboxylate (1.95 g, 6.30 mmol) in DMF (50 mL) and DME (6.9 mL), was added sodium carbonate in water (2M, 6.3 mL). The mixture was degassed for 15 min. Dichloro[bis(diphenylphosphino)ferrocene]palladium(II) CH2Cl2 adduct (307 mg, 0.42 mmol) was added. The mixture was stirred at 80° C. under nitrogen overnight then cooled to rt. The mixture was filtered through Celite®, washing with EtOAc (100 mL) then 20% MeOH/DCM (100 mL). The filtrate was concentrated to dryness. ISCO® purification (20% EtOAc/hexane then EtOAc) afforded title compound (1.0 g, 69.4%). 1H NMR (400 MHz, DMSO-d6) δ 8.20 (s, 2H), 7.97 (s, 1H), 7.34 (s, 1H), 6.38 (t, 1H), 4.02 (d, 2H), 3.58 (t, 2H), 2.62 (t, 2H), 1.41 (s, 9H); LC-MS m/z [M+H]+ 341.2, RT 3.16 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-f183d02adec74d4b918f2b06c664b7f0
Source noteuspto-grants-2013_04