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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898444Generated: November 2, 2026

4-Bromoaniline → HCID 178432345, compound

https://huagongshe.com/reaction/1898444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178432356HCID 178432356—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178432345HCID 17843234515%

Reaction Steps

The title compound was prepared following the procedure as described for Example-177 using 7-[(2,6-dichlorophenyl)amino]-2-methyl-8H-imidazo[4,5-e][1,3]benzoxazole-4-carboxylic acid (Intermediate-55, 0.100 g, 0.276 mmol), benzene (4 mL), thionyl chloride (5.0 mL), 4-bromo aniline (0.142 g, 0.828 mmol), THF (5.0 mL) and 60% NaH (0.033 g, 0.825 mmol). The obtained product was further purified by column chromatography on neutral alumina eluting with 1.5-2.0% MeOH:DCM to afford 0.022 g of the desired product. 1HNMR (DMSO-d6): δ 2.70 (s, 3H), 6.54 (s, 1H), 6.67 (d, J=8.4 Hz, 1H), 6.83 (s, 1H), 6.98 (d, J=8.1 Hz, 1H), 7.12-7.26 (m, 2H), 7.33-7.38 (m, 2H), 8.61 (s, 1H), 9.04 (s, 1H); MS [M+H]+: 532.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-6c2fa39367ce401e8f9773c7a49981e0
Source noteuspto-grants-2013_08