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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373879Generated: October 30, 2026

1,2-Dichloroethane → HCID 178485734, compound

https://huagongshe.com/reaction/2373879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 178508471HCID 178508471—
SolventDimethylformamideHCID 6228—
ProductHCID 178485734HCID 17848573457.3%

Reaction Steps

General procedure to EXAMPLES 37 and 38: A DMF solution (2 mL) of acid trans-4-[8-amino-1-(3-benzyloxy-phenyl)-imidazo[1,5-a]pyrazin-3-yl]-cyclohexanecarboxylic acid (100 mg, 0.23 mmol) and methylamine hydrochloride (153 mg, 2.26 mmol) in a sealed tube was charged with DIEA (394 μL, 2.26 mmol), 0.6 M HOAt in DMF (377 μL, 0.23 mmol), and then EDC (65 mg, 0.34 mmol). The reaction mixture stirred at rt for 16 h. The reaction mixture was concentrated to solids, taken up in CH2Cl2, charged with silica, and concentrated to brown solids. The crude material was purified by silica gel column chromatography [Jones Flashmaster, 20 g/70 mL cartridge, eluting with 2% ˜7 N NH3 in MeOH/CH2Cl2 to 5% ˜7 N NH3 in MeOH/CH2Cl2] to afford trans-4-[8-amino-1-(3-benzyloxy-phenyl)-imidazo[1,5-a]pyrazin-3-yl]-cyclohexanecarboxylic acid methylamide as an off-white solid (60 mg, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459554B2
Source datasetuspto-grants-2008_12
ORD IDord-059db909cd144a3d97b25fce62620d92
Source noteuspto-grants-2008_12