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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221204Generated: October 27, 2026

Hydrochloric Acid → 1-(1-methyl-1H-imidazol-4-ylsulfonyl)azetidine-3-carbonitrile

https://huagongshe.com/reaction/221204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-methyl-1H-imidazole-4-sulfonyl chlorideHCID 2736887—
Reactant1-Boc-3-cyanoazetidineHCID 10631283—
Solvent1,4-DioxaneHCID 31275—
Product1-(1-methyl-1H-imidazol-4-ylsulfonyl)azetidine-3-carbonitrileHCID 5953449280%

Reaction Steps

To a solution of 1-N-Boc-3-cyanoazetidine (5.0 g, 27.5 mmol) in 1,4-dioxane (50 mL) was added 4 N HCl (50 mL) and stirred for 2 h. The reaction was concentrated under vacuum. The residue was dissolved in CH2Cl2 (60 mL) and DIPEA (10.6 mL, 60.4 mmol) and added 1-methylimidazole-4-sulfonyl chloride (4.94 g, 27.5 mmol) and stirred at room temperature for 20 h. The reaction mixture was washed with 2 N NaOH (50 mL), dried over MgSO4 and concentrated under vacuum to afford 8 as a white crystalline solid (4.97 g, 80%); 1H-nmr (300 MHz, CDCl3) δ 7.06 (s, 1H), 7.56 (s, 1H), 4.27-4.19 (m, 4H), 3.82 (s, 3H), 3.43-3.31 (m, 1H); LC-MS (214) 99%, 0.93 min, m/z 227.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207155B2
Source datasetuspto-grants-2012_06
ORD IDord-813792d6910d47c09ead3188c7288b7d
Source noteuspto-grants-2012_06