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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258154Generated: October 31, 2026

1-(Bromomethyl)-3-chlorobenzene → HCID 59253658, compound

https://huagongshe.com/reaction/1258154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59253661HCID 59253661—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 59253658HCID 5925365839.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-(piperidin-4-ylamino)-pyridazine-3-carbonitrile (D3) (0.150 g, 0.74 mmol), 3-chlorobenzyl bromide (0.102 ml, 0.78 mol) and diisopropylethylamine (0.196 ml, 1.11 mol) in acetonitrile (2 ml) was stirred at 120° C. for 5 min., under microwave irradiation (Biotage MW-oven). The reaction mixture was then diluted with dichloromethane and extracted with a saturated solution of sodium carbonate. The organic layers were separated, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The residue was then purified by column chromatography (silica gel; 0-2.5% ammonia in methanol (7 M)/dichloromethane). The desired fractions were collected and evaporated in vacuo, and the residue triturated with diisopropylether to yield E13 (0.095 g, 39%) as a white solid. C17H18ClN5 requires 327. Found 328 (MH+); mp: 151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-ff038c9b23b343b89baef3bfdb43f476
Source noteuspto-grants-2013_06