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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585647Generated: November 3, 2026

Water → HCID 21219160, compound

https://huagongshe.com/reaction/1585647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1-Dimethylethyl 4-(4-phenyl-1H-1,2,3-triazol-1-yl)-1-piperidinecarboxylateHCID 12160909—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 21219160HCID 212191607.9%

Reaction Steps

To a solution of N-t butyloxycarbonyl-4-((4-phenyl)triazol-1-yl)piperidine (2.5 g) in a 1:1 mixture of diethyl ether and methanol (10 ml) was added a solution of hydrogen chloride in methanol (10 ml, ~5 mol) and the reaction mixture was stirred at room temperature for 72 hrs. The solid was filtered off and dried then redissolved in N,N-dimethylformamide (20 ml), to which was added benzyl bromide (0.4 ml, 3.4 mmol) and ethyldiisopropylamine (0.55 ml, 3.4 mmol). The reaction mixture was stirred at room temperature for 18 hrs under nitrogen, then poured into water (200 ml) and extracted with dichloromethane (3×100 ml). The combined organic layers were washed with brine (2×50 ml), dried (MgSO4), filtered and concentrated under vacuum. The residue was purified by flash silica chromatography using methanol in dichloromethane (0-4%) and ammonia (0.5%). The product obtained was redissolved in a 1:1 mixture of diethyl ether and methanol (5 ml) with hydrogen chloride in methanol (10 ml, ~5 mol). After 5 mins the solvent was removed under vacuum and the residue was recrystallized from methanol and ethyl acetate to give the required product as a white solid (85 mg). M.p 206-280° C. 1H NMR (DMSO) δ 2.11 (4H,m), 2.60 (2H,m), 2.77 (2H,m), 3.04 (2H,m), 4.52 (1H,m), 7.18-7.85 (11H,m). MS (CI) m/e 319 [MH]+. Anal. Found C, 64.90; H, 6.43; N, 15.05. C20H22N4.HCl.0.75H2O requires C, 65.21; H, 6.70; N, 15.21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939436
Source datasetuspto-grants-1999_08
ORD IDord-20ca0d28f5e74691b1793b0a0346d868
Source noteuspto-grants-1999_08