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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631670Generated: October 26, 2026

Phenyl chloroformate → phenyl 3-tert-butyl-1-(pyridin-3-yl)-1H-pyrazol-5-ylcarbamate

https://huagongshe.com/reaction/631670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl chloroformateHCID 15891—
Reactant3-(Tert-butyl)-1-(3-pyridyl)pyrazole-5-amineHCID 46196775—
Productphenyl 3-tert-butyl-1-(pyridin-3-yl)-1H-pyrazol-5-ylcarbamateHCID 6687685895.1%

Reaction Steps

Following the procedure in Example 118A, 3-tert-butyl-1-(pyridin-3-yl)-1H-pyrazol-5-amine (665 mg, 3.08 mmol) and phenyl chloroformate (705 mg, 4.5 mmol) were reacted to give phenyl 3-tert-butyl-1-(pyridin-3-yl)-1H-pyrazol-5-ylcarbamate (984 mg, 2.93 mmol, 95%). 1H NMR (300 MHz, DMSO-d6) δ 7.42-7.39 (m, 3H), 7.30-7.26 (m, 5H), 6.85 (t, 1H), 6.82 (d, 2H), 1.21 (s, 9H); LC-MS (ESI) m/z 337 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-e790e07e111d45f4a85a62e5d3e92c7e
Source noteuspto-grants-2016_04