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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262198Generated: November 3, 2026

4-Bromo-1,2-dimethyl-1H-imidazole → [7-(1,2-Dimethyl-1H-imidazol-4-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(4-morpholin-4-yl-phenyl)-amine

https://huagongshe.com/reaction/1262198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1,2-dimethyl-1H-imidazoleHCID 7204875—
ReactantN-[4-(Morpholin-4-yl)phenyl]-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrolo[2,1-f][1,2,4]triazin-2-amineHCID 57416041—
Product[7-(1,2-Dimethyl-1H-imidazol-4-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(4-morpholin-4-yl-phenyl)-amineHCID 46851712—

Reaction Steps

[7-(1,2-Dimethyl-1H-imidazol-4-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-(4-morpholin-4-yl-phenyl)-amine was prepared from 4-bromo-1,2-dimethyl-1H-imidazole and (4-morpholin-4-yl-phenyl)-[7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl]-amine in an analogous manner to Example 1042b. Product isolated as a yellow solid (11 mg, 10%). m.p.=decomposed at 250° C.; LCMS (m/e) 390 (M+H); 1H-NMR (CDCl3, 400 MHz) δ 8.62 (s, 1H), 7.85 (s, 1H), 7.55 (d, 2H, J=8.9 Hz), 7.27-7.23 (m, 1H), 6.97 (d, 2H, J=8.9 Hz), 6.81 (d, 1H, J=4.8 Hz), 6.56 (bs, 1H), 3.93-3.87 (m, 4H), 3.64 (s, 3H), 3.18-3.12 (m, 4H), 2.46 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-8056ed4919614a06b29adbd2d5724bf1
Source noteuspto-grants-2013_06