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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555909Generated: October 30, 2026

Benzoyl chloride, 3-chloro- → HCID 178522173, compound

https://huagongshe.com/reaction/555909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantHCID 178507674HCID 178507674—
ProductHCID 178522173HCID 17852217313%

Reaction Steps

The title compound was prepared essentially according to the method of Example 4, but using 5-Chloro-2-(1H-tetrazol-5-yl)aniline (1.0 mmol) and 3-chlorobenzoyl chloride. After precipitation, the product was further purified by reverse phase C18 preparative HPLC (water/acetonitrile w/0.1% formic acid, 30%-100% eluant gradient) to yield the desired product (46.0 mg, 13%). 1H NMR (400 MHz, d6-DMSO): δ 13.07 (s, 1H), 8.87 (s, 1H), 8.29 (s, 1H), 8.17 (s, 1H), 7.76 (m, 2H), 7.27 (s, 1H), 6.96 (s, 2H). MS (EI) for C14H9Cl2N5O: 334.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053454B2
Source datasetuspto-grants-2011_11
ORD IDord-931dd42bdb274fe999f16604ba74f2c9
Source noteuspto-grants-2011_11