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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736818Generated: October 26, 2026

methyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylate → methyl (1S,2R)-2-amino-1-methylcyclopentanecarboxylate

https://huagongshe.com/reaction/736818

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylateHCID 86607912—
CatalystPalladiumHCID 23938—
SolventFormic acid methanolHCID 18963719—
Productmethyl (1S,2R)-2-amino-1-methylcyclopentanecarboxylateHCID 8660791393.2%

Reaction Steps

According to the procedure of Example 53, Step 2, using methyl (1S,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-methylcyclopentanecarboxylate (1.025 g, 2.92 mmol), 4.4% HCO2H/MeOH (30 mL) and 10% Pd/C (1.058 g), methyl (1S,2R)-2-amino -1-methylcyclopentanecarboxylate (527 mg, 2.72 mmol, 93%) was obtained as a colorless solid. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.29 (s, 3H) 1.56-1.62 (m, 1H) 1.64-1.76 (m, 3H) 2.07-2.13 (m, 1H) 2.15-2.22 (m, 1H) 3.24-3.31 (m, 1H) 3.64-3.71 (m, 3H) 8.18 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595327B2
Source datasetuspto-grants-2009_09
ORD IDord-fbc15acac26747b2a9494d0fb8823780
Source noteuspto-grants-2009_09