Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389612Generated: November 1, 2026

benzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamate → 6-(4-Cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine

https://huagongshe.com/reaction/389612

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamateHCID 66851549—
CatalystPalladiumHCID 23938—
Product6-(4-Cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amineHCID 58102966100.2%

Reaction Steps

A mixture of benzyl 6-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-ylcarbamate (660 mg, 1.96 mmol, 1.0 eq) and Pd/C (80 mg 10% Pd loading, 40 mg/mmol) was loaded into a flask and purged with nitrogen. Ethanol (0.4 M) was added and the flask was charged with hydrogen (1 atm—balloon pressure). The reaction was stirred at room temperature for 90 minutes, and judged to be complete by TLC. The reaction mixture was filtered through celite, and concentrated under reduced pressure to give 395 mg (95%) of 6-(4-cyclopropyl-4H-[1,2,4]triazol-3-yl)-pyridin-2-ylamine. C10H11N5. 202.1 (M+1). 1H NMR (DMSO) d 8.14 (s, 1H), 7.54 (t, J=8 Hz, 1H), 7.46 (d, J=7 Hz, 1H), 6.60 (d, J=8 Hz, 1H), 4.70 (br s, 2H), 3.85-3.88 (m, 1H), 1.04-1.07 (m, 2H), 0.85-0.88 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378108B2
Source datasetuspto-grants-2013_02
ORD IDord-59f6cf71b31e4762a547369128e747f1
Source noteuspto-grants-2013_02