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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972880Generated: October 31, 2026

7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amine → HCID 58529670, compound

https://huagongshe.com/reaction/1972880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromopyrrolo[2,1-f][1,2,4]triazin-4-amineHCID 42281383—
Reactanttert-Butyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 53302321—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium CarbonateHCID 10340—
ProductHCID 58529670HCID 5852967098.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butylester (4 g, 11 mmol) and 7-bromo-pyrrolo[2,1-f][1,2,4]triazin-4-ylamine (1.3 g, 6.1 mmol) in DME (133 mL) and 2 N Na2CO3 solution (26 mL) was added Pd(dppf)Cl2 (452 mg, 0.6 mmol). The reaction mixture was degassed with N2 for 15 min. The mixture was heated to 80° C. for 23 h. The reaction mixture was filtered through a pad of Celite® and the filtrate was concentrated in vacuo. The crude residue was purified by Biotage® to provide 2.20 g (55%) of the desired product. 1H NMR (300 MHz, DMSO-d6) δ 7.9 (m, 2 H), 7.85 (d, 1 H), 7.2 (d, 1 H), 7.0 (d, 2 H), 4.5 (s, 2 H), 3.5 (t, 2 H), 2.8 (t, 2 H) 1.4 (s, 9 H); ES-MS m/z 366.05 [M+H]+, HPLC RT (min) 2.64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-19a956df8eff4eddb8f0b2215892d47c
Source noteuspto-grants-2013_04