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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Bromomethyl)-3-chlorobenzene | HCID 69838 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59253661 | HCID 59253661 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59253658 | HCID 59253658 | 39.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466153B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ff038c9b23b343b89baef3bfdb43f476 |
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| Source note | uspto-grants-2013_06 |
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