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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178590Generated: October 29, 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/2178590

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 numberUS09067933B2
Source datasetuspto-grants-2015_06
ORD IDord-4c28c5ffa24e48cdbb95fd587b508064
Source noteuspto-grants-2015_06