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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914737Generated: October 30, 2026

3,6-Dichloro-4-methylpyridazine → HCID 16748608, compound

https://huagongshe.com/reaction/914737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-Dichloro-4-methylpyridazineHCID 87923—
Reactant(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptaneHCID 11521263—
ProductHCID 16748608HCID 1674860856%

Reaction Steps

3,6-Dichloro-4-methylpyridazine (Aldrich Chemical Company) and tert-butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate, prepared as described in (J. Med. Chem., (1988) 31, 1598-1611), were processed as described in Example 2A to provide the title compound (56% yield). 1H NMR (CDCl3, 300 MHz) δ 1.41 (s, 4.5H), 1.43 (s, 4.5H), 1.90-2.09 (m, 2H), 2.31(s, 3H), 3.35-3.45 (m, 3H), 3.53-3.60(m, 1H), 4.56(s, 0.5H), 4.69(s, 0.5H), 4.90(s, 0.5H), 5.08(s, 0.5H), 6.48(s, 1H); MS (DCI/NH3) m/z 325 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265115B2
Source datasetuspto-grants-2007_09
ORD IDord-e912f2c641104e2387d183c83a33c1b2
Source noteuspto-grants-2007_09