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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43966Generated: October 29, 2026

Methanol → Methyl cis(+/-)-5-(4-amino-3-methoxypiperidin-1-yl)-2-methoxybenzoate

https://huagongshe.com/reaction/43966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl cis(+/-)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-methoxybenzoateHCID 86648847—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
ProductMethyl cis(+/-)-5-(4-amino-3-methoxypiperidin-1-yl)-2-methoxybenzoateHCID 86648848—

Reaction Steps

The same operation as in Example (40e) was performed using methyl cis(±)-5-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-methoxybenzoate obtained in Example (258a) (35 mg, 0.08 mmol), a 10% palladium-carbon catalyst (9 mg), methanol (1.5 mL) and ethyl acetate (1.5 mL), to obtain the title compound. The resulting compound was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-e5ee5cf50c4f4d93b3d9fe133cbb4f87
Source noteuspto-grants-2013_09