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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157797Generated: October 30, 2026

Sodium Azide → HCID 68692912, compound

https://huagongshe.com/reaction/1157797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 68691865HCID 68691865—
CatalystMercuric ChlorideHCID 24085—
SolventDimethylformamideHCID 6228—
ProductHCID 68692912HCID 6869291284.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

Part C: To a solution of tert-butyl 4-(methylthio(pyridin-2-ylimino)methyl)piperazine-1-carboxylate (12.00 g, 36.0 mmol) in DMF (200 mL) at 25° C. was added sodium azide (11.60 g, 178 mmol), followed by mercury(II)chloride (10.90 g, 40.0 mmol), and the resulting mixture was stirred at 25° C. for 19 d. The mixture then was filtered, and the solids were washed with DMF. The combined filtrate was concentrated under vacuum, and the residue was diluted with ethyl acetate. The resulting mixture was filtered again. The filtrate was washed with water (×3) and brine, dried over anhyd. sodium sulfate, filtered, and concentrated. Column chromatography on silica gel (elution: 0-20% diethyl ether/methylene chloride) to afford tert-butyl 4-(1-(pyridin-2-yl)-1H-tetrazol-5-yl)piperazine-1-carboxylate (10.10 g) as an off-white solid, following crystallization from a mixture of 1-chlorobutane/hexane; Mass Spec.: m/e: 332.11 (M+H)+ [calc'd: 332.17]; 1HNMR (300 MHz, CDCl3) δ 8.57 (m, 1H), 7.94 (m, 1H), 7.79 (d, 1H, J=8 Hz), 7.40 (m, 1H), 3.52 (m, 4H), 3.34 (m, 4H), 1.43 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807676B2
Source datasetuspto-grants-2010_10
ORD IDord-2cfb66c28be14092b314b047d56a32b3
Source noteuspto-grants-2010_10