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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887146Generated: October 27, 2026

2-Chloropropane → 1-Isopropyl-4-[6-(4-trifluoromethylphenyl)pyridazin-3-yl]-[1,4]diazepane, dihydrochloride

https://huagongshe.com/reaction/1887146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropropaneHCID 6361—
ReactantTriethylamineHCID 8471—
ReactantSodium hydrideHCID 24758—
Reactant4-[6-(4-Trifluoromethylphenyl)pyridazin-3-yl][1,4]diazepane, dihydrochlorideHCID 131730778—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-Isopropyl-4-[6-(4-trifluoromethylphenyl)pyridazin-3-yl]-[1,4]diazepane, dihydrochlorideHCID 13173077721%

Reaction Steps

4-[6-(4-Trifluoromethylphenyl)pyridazin-3-yl]-[1,4]diazepane, dihydrochloride (0.028 g, 0.071 mmol) was suspended in THF (4 mL) and triethylamine (0.022 g, 0.21 mmol) was added. Sodium hydride (0.0085 g, 0.35 mmol) was added and the reaction mixture was stirred at rt for 20 min. Dry N,N-dimethylformamide (1 mL) and 2-chloropropane (0.056 g, 0.71 mmol) was added and the reaction mixture was heated 30 min at 160° C. and 30 min at 180° C. in a microwave oven. The reaction mixture was purified on a silicagel column (0.04-0.063 mesh) using dichloromethane/MeOH (9:1) as eluent. This afforded a crude oil containing several components that was purified further by preparative HPLC using Method B. This afforded 9 mg of an oil which was dissolved into MeOH. Addition of HCl in diethyl ether afforded 6.5 mg (21%) of the title compound as an oily dihydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501739B2
Source datasetuspto-grants-2013_08
ORD IDord-d4d843959eb3441dab3cb2dd9318b25e
Source noteuspto-grants-2013_08