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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74433Generated: October 26, 2026

N,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine → HCID 178454244, compound

https://huagongshe.com/reaction/74433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-Bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidineHCID 4428040—
Reactant(3-(Cyclohexylmethoxy)phenyl)methanamineHCID 28368432—
SolventAcetonitrileHCID 6342—
ProductHCID 178454244HCID 178454244—

Reaction Steps

A solution of N,N′-bis(tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine (0.71 g, 2.28 mmol) and (3-(cyclohexylmethoxy)phenyl)methanamine (0.50 g, 2.28 mmol) in acetonitrile (15 ml) was stirred at 50° C. for 18 h under argon. After cooling to room temperature, a white solid was formed, collected via filtration, and dried under vacuum to give (Z)-tert-butyl(tert-butoxycarbonylamino)(3-(cyclohexylmethoxy)benzylamino)methylenecarbamate. Yield (400 mg, 38%). 1H NMR (400 MHz, DMSO-d6) δ 11.47 (s, 1H), 8.61 (t, J=6.0 Hz, 1H), 7.20 (t, J=8.0 Hz, 1H), 6.77-6.86 (m, 3H), 4.44 (d, J=5.6 Hz, 2H), 3.72 (d, J=6.4 Hz, 2H), 1.60-1.80 (m, 6H), 1.45 (s, 9H), 1.36 (s, 9H), 0.95-1.25 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829244B2
Source datasetuspto-grants-2014_09
ORD IDord-dc8bca16759e49cab52c42b5d267bbcc
Source noteuspto-grants-2014_09