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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262436Generated: November 2, 2026

[3-(Hydroxymethyl)phenyl]boronic acid → HCID 66712385, compound

https://huagongshe.com/reaction/1262436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
ReactantHCID 66711673HCID 66711673—
ProductHCID 66712385HCID 6671238520%

Reaction Steps

Analogous to Example 1504, (7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-[3-(4-methyl-piperazin-1-yl)-phenyl]-amine (0.0731 g, 0.189 mmol) and (3-Hydroxymethylphenyl)boronic acid (0.0513 g, 0.338 mmol) were reacted to afford (3-{2-[3-(4-Methyl-piperazin-1-yl)-phenylamino]-pyrrolo[2,1-f][1,2,4]triazin-7-yl}-phenyl)-methanol as a yellow powder (15 mg, 20%). LCMS: 415 (M+H); 1H-NMR (CDCl3): 8.70 (s, 1H), 8.21 (s, 1H), 7.92 (s, 1H), 7.62 (d, 1H, J=6.96 Hz), 7.49 (m, 2H), 7.20 (t, 1H, J=8.19 Hz), 6.93 (d, 1H, J=4.50 Hz), 6.88 (s, 1H), 6.84 (d, 1H, J=4.50 Hz), 6.87 (d, 1H, J=8.19 Hz), 4.77 (s, 2H), 2.98 (t, 4H, J=4.96 Hz), 2.44 (t, 4H, J=4.96 Hz), 2.34 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-d5dde63e089e4a24bd40b8e4920a3ee6
Source noteuspto-grants-2013_06