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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040227Generated: October 31, 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/1040227

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 numberUS08552196B2
Source datasetuspto-grants-2013_10
ORD IDord-5c7fc459bb754138b85d04f43c5bc389
Source noteuspto-grants-2013_10