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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965851Generated: November 2, 2026

Bromomethyl 4-methoxyphenyl ketone → HCID 59283110, compound

https://huagongshe.com/reaction/1965851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
Reactant6-Methoxy-1H-indazol-3-amineHCID 21409192—
ProductHCID 59283110HCID 59283110—

Reaction Steps

Compound 7-methoxy-2-(4-methoxyphenyl)-5H-imidazo[1,2-b]indazole (W302) was prepared using the general procedure for cyclization between 6-methoxy-1H-indazol-3-amine (90 mg, 0.3 mmol) and 2-bromo-1-(4-methoxyphenyl)ethanone (72 mg, 0.31 mmol), as white solid (50 mg, 57%). 1H NMR (400 MHz, DMSO-d6) δ 8.57 (s, 1 HO, 7.85-7.81 (m, 3 H), 7.16-7.12 (m, 3 H), 6.99 (dd, J=8.8, 2.4 Hz, 1 H), 3.90 (s, 3 H), 3.84 (s, 3 H); MS (ESI) m/z 294 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420052B2
Source datasetuspto-grants-2013_04
ORD IDord-f7ec84a7ee414c7a810c217385c74ee3
Source noteuspto-grants-2013_04