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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79108Generated: October 29, 2026

3,6-Dichloropyridazine → HCID 58299919, compound

https://huagongshe.com/reaction/79108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-DichloropyridazineHCID 67331—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
SolventEthyl AcetateHCID 8857—
ProductHCID 58299919HCID 5829991982%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3,6-dichloropyridazine (298 mg, 2 mmol) and (R)-1-N-Boc-2-methyl piperazine (401 mg, 2.0 mmol) in N,N-diisopropylethylamine (0.7 mL, 4 mmol) was stirred at 120° C. for 5 h. The reaction mixture was diluted with ethyl acetate and washed with brine (2×), then dried over MgSO4. The salts were removed by filtration and the filtrate was concentrated and the residue was purified by chromatography on silica gel eluting with 20% to 80% ethyl acetate in hexane to give compound 11 as a light yellow solid (511 mg, 82%). 1H NMR (500 MHz, CD3OD) δ 7.24 (1H, d, J=10 Hz), 6.88 (1H, d, J=10 Hz), 4.38 (1H, br s), 4.17 (1H, d, J=10 Hz), 4.05-3.97 (2H, m), 3.39 (1H, dd, J=15 Hz, J=5 Hz), 3.29 (1H, ddd, J=15 Hz, J=10 Hz, J=5 Hz), 1.51 (9H, s), 1.21 (3H, d, J=10 Hz) ppm; LCMS-ESI (POS), M/Z, M+1: Found 313.1, Calculated 313.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841312B2
Source datasetuspto-grants-2014_09
ORD IDord-dfa92a3061aa48999be4e36e5879368c
Source noteuspto-grants-2014_09