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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500493Generated: November 4, 2026

2,4-Dichlorobenzylamine → HCID 178508416, compound

https://huagongshe.com/reaction/1500493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzylamineHCID 1485—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178508418HCID 178508418—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178508416HCID 17850841651.9%

Reaction Steps

To a suspension of 2-amino-4-hydroxypyrimidine-5-carboxylic acid (311 mg), (2,4-dichlorophenyl)methanamine (353 mg), and triethylamine (2.8 mL) in N,N-dimethylformamide (8 mL), 2-(1H-7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (839 mg) was added at room temperature, and the mixture was stirred for 90 minutes. 2,4-Dichlorobenzylamine (353 mg) and 2-(1H-7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (839 mg) were added thereto, and the mixture was stirred for 12 hours. A saturated aqueous ammonium chloride solution was added to the reaction solution, and the mixture was stirred for 1 hour and then filtered. The product collected by filtration was washed with water, dried under reduced pressure, and then suspended in ethyl acetate. This suspension was shaken for 1 hour in an ultrasonic bath and then filtered. The obtained product collected by filtration was dried under reduced pressure to obtain the title compound (326 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206168B2
Source datasetuspto-grants-2015_12
ORD IDord-668d08ee3e8c4c43b3ef1dd99f2eb7ce
Source noteuspto-grants-2015_12