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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401213Generated: November 1, 2026

Hydrazine → HCID 178432644, compound

https://huagongshe.com/reaction/1401213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant5-Bromo-6-methylpicolinamideHCID 66607724—
SolventAcetic AcidHCID 176—
ProductHCID 178432644HCID 178432644—

Reaction Conditions

Temperature85 °C

Reaction Steps

5-Bromo-6-methylpicolinamide (1 g, 4.65 mmol) and N,N-dimethylformamide dimethylacetal (20 mL) were combined in a 100 mL round-bottom flask with a stir bar and heated at 85° C. under a reflux condenser under nitrogen for 3 h. The resulting mixture was concentrated under reduced pressure and dried under vacuum to give yellow oil, which was used in the next step without purification. The residue was diluted with acetic acid (10 mL) and hydrazine (2.5 mL, 70.3 mmol) was added drop-wise and allowed to stir at room temperature for 5 h. The reaction mixture was poured into ice water. The resulting solid was filtered, washed with water and dried to give the desired product as a white solid. The aqueous filtrate was extracted with dichloromethane. The organic layer was concentrated under reduced pressure nearly to dryness to yield additional material. Combination of two batches gave the desired product (0.7 g, 2.9 mmol, 63% yield). MS (ESI) m/z 241.1 [M+2]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907087B2
Source datasetuspto-grants-2014_12
ORD IDord-b2c59b70a39e47c09a0e458e6fd8a4aa
Source noteuspto-grants-2014_12