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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898445Generated: October 30, 2026

Thionyl Chloride → HCID 178432346, compound

https://huagongshe.com/reaction/1898445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantHCID 178432356HCID 178432356—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178432346HCID 17843234610.7%

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-tert-butylaniline (0.123 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 0.015 g of the desired product. 1HNMR (DMSO-d6): δ 1.28 (s, 9H), 2.65 (s, 3H), 6.54 (s, 1H), 7.37 (d, J=7.8 Hz, 3H), 7.60-7.68 (m, 4H), 9.43 (s, 1H), 9.93 (s, 1H), 11.56 (s, 1H); MS [M+H]+: 508.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519149B2
Source datasetuspto-grants-2013_08
ORD IDord-c377308c296e4e5bb9ef8c886b3b0079
Source noteuspto-grants-2013_08