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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987191Generated: October 30, 2026

Methyl {3-nitro-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}carbamate → Methyl {3-amino-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}carbamate

https://huagongshe.com/reaction/1987191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl {3-nitro-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}carbamateHCID 57723218—
SolventEthyl AcetateHCID 8857—
SolventPalladiumHCID 23938—
ProductMethyl {3-amino-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}carbamateHCID 57723219—

Reaction Steps

Methyl {3-nitro-4-[(tetrahydro-2H-pyran-4-ylmethyl)amino]phenyl}carbamate (2.53 g, 8.18 mmol) was dissolved in 50 mL of EtOAc containing a catalytic amount of 10% Pd/C. The solution was shaken under H2 atmosphere (40 psi) using a Parr hydrogenation apparatus overnight at rt. The solution was filtered through Celite and the solvent was evaporated. Yield: 2.29 g (99%). 1H NMR (400 MHz, CHLOROFORM-D) δ 1.40 (m, 2 H), 1.70-1.74 (m, 1 H), 1.74-1.77 (m, 1 H), 1.81-1.92 (m, 1 H), 2.99 (d, J=6.64 Hz, 2 H), 3.34 (br.s, 2 H), 3.41 (m, 2 H), 3.74 (s, 3 H), 3.99 (d, J=3.51 Hz, 1 H), 4.02 (d, J=3.51 Hz, 1 H), 6.38 (br.s, 1 H), 6.55-6.60 (m, 1 H), 6.62-6.68 (m, 1 H), 6.95 (br.s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550495B2
Source datasetuspto-grants-2009_06
ORD IDord-b5ac6657a8e4452392457cb4ddc5b942
Source noteuspto-grants-2009_06