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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655268Generated: November 1, 2026

Hydrazine → (3-Bromo-5,7-difluoro-quinolin-6-yl)-acetic acid hydrazide

https://huagongshe.com/reaction/655268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 2-(3-bromo-5,7-difluoroquinolin-6-yl)acetateHCID 59320329—
Reactant2-(3-Bromo-5,7-difluoroquinolin-6-yl)acetic acidHCID 59320439—
SolventMethanolHCID 887—
Product(3-Bromo-5,7-difluoro-quinolin-6-yl)-acetic acid hydrazideHCID 59320448402.6%

Reaction Steps

SOCl2 (394 mg, 3.31 mmol) was added dropwise to a stirred solution of (3-bromo-5,7-difluoro-quinolin-6-yl)-acetic acid (500 mg, 1.65 mmol) in 12 ml of methanol at 0° C. under N2. After stirring for 2 hours at room temperature the solvent was evaporated and the crude (3-bromo-5,7-difluoro-quinolin-6-yl)-acetic acid methyl ester was used directly in the next step. To a mixture of (3-bromo-5,7-difluoro-quinolin-6-yl)-acetic acid methyl ester (2.29 g, 7.22 mmol) in methanol (100 mL) was added anhydrous hydrazine (2.31 g, 72.2 mmol). The mixture was heated at 55° C. for 4 hours. Additional anhydrous hydrazine (1.16 g, 36.1) was added and the mixture was heated at 55° C. for 2 hours. The reaction mixture was cooled to room temperature to give a white solid. The white solid was filtered and washed with cold methanol to obtain 2.1 g of the title compound (92% yield). MS: m/z 318 [M+H+]. 1H NMR (500 MHz. DMSO-d6): δ 1.99 (2H, s), 4.25 (2H, bs), 7.72 (1H, d), 8.74 (1H, s), 9.03 (1H, s), 9.35 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071581B2
Source datasetuspto-grants-2011_12
ORD IDord-81d7f29af2364e4f91899f89741279bb
Source noteuspto-grants-2011_12