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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475294Generated: October 31, 2026

HCID 86723936, compound → HCID 86723935, compound

https://huagongshe.com/reaction/1475294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86723936HCID 86723936—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 86723935HCID 8672393578.1%

Reaction Steps

Pd/C (10%, 810 mg) was added to a solution of (2R,5S)-4-benzyloxycarbonylmethyl-5-ethyl-2-methyl-piperazine-1-carboxylic acid tert-butyl ester (2.8 g, 7.6 mmol) in MeOH (50 mL). The suspension was stirred overnight under H2. and catalyst was removed via filtration through Celite and the filtrate was evaporated in vacuo to give the title compound (1.7 g) as a pale yellow solid. 1H NMR (DMSO-d6): 4.41-3.89 (1H, m), 3.89-3.64 (1H, m), 3.37-3.21 (1H, m), 3.21-3.05 (2H, m), 2.71-2.55 (2H, m), 2.54-2.42 (3H, m), 1.45-1.36 (9H, m), 1.16 (3H, d), 0.83 (3H, t). MS: [M+H]+=287.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018214B2
Source datasetuspto-grants-2015_04
ORD IDord-c9104f2108574f53a958b173f5025dcd
Source noteuspto-grants-2015_04