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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089381Generated: October 31, 2026

Tert-butyl (piperidin-4-ylmethyl)carbamate → tert-butyl (1-(1-(cyclopropylmethyl)-4-nitro-1H-pyrazol-5-yl)piperidin-4-yl)methylcarbamate

https://huagongshe.com/reaction/2089381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
Reactant5-Chloro-1-(cyclopropylmethyl)-4-nitro-1h-pyrazoleHCID 58464813—
Producttert-butyl (1-(1-(cyclopropylmethyl)-4-nitro-1H-pyrazol-5-yl)piperidin-4-yl)methylcarbamateHCID 5846503395%

Reaction Steps

Reaction of 5-chloro-1-cyclopropylmethyl-4-nitro-1H-pyrazole and tert-butyl piperidin-4-ylmethylcarbamate gave tert-butyl (1-(1-(cyclopropylmethyl)-4-nitro-1H-pyrazol-5-yl)piperidin-4-yl)methylcarbamate as a pale yellow gum (0.57 g, 95%). 1H NMR (400 MHz, CDCl3) δ 8.07-8.03 (m, 1H), 4.63 (s, 1H), 3.91 (d, J=7.1 Hz, 2H), 3.40-3.32 (m, 2H), 3.13-3.06 (m, 2H), 2.95 (d, J=11.5 Hz, 2H), 1.81 (d, J=12.9 Hz, 2H), 1.46 (s, 9H), 1.42-1.14 (m, 3H), 0.95-0.82 (m, 1H), 0.63-0.57 (m, 2H), 0.42-0.35 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436001B2
Source datasetuspto-grants-2013_05
ORD IDord-4a29fa60f2784f8d843d045d81df46a1
Source noteuspto-grants-2013_05