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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481722Generated: October 31, 2026

HCID 71281757, compound → HCID 71281824, compound

https://huagongshe.com/reaction/1481722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71281757HCID 71281757—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 71281824HCID 71281824—

Reaction Steps

Solution of 1-benzyl 4-tert-butyl 2-(5-(3-ethyl-6-methoxy-5-(methoxycarbonyl)pyridin-2-yl)-1-methyl-1H-indol-2-yl)piperazine-1,4-dicarboxylate (71.4 mg, 0.11 mmol), prepared according to procedure described in Example 67, Step 3, in MeOH (1 mL) was hydrogenated over Pd/C (10% Degussa type, 10 mg) with H2-balloon. After 1 h complete consumption of starting material was observed. Catalyst was filtered and washed with MeOH (5 mL). Concentration of mother liquor afforded tert-butyl 3-(5-(3-ethyl-6-methoxy-5-(methoxycarbonyl)pyridin-2-yl)-1-methyl-1H-indol-2-yl)piperazine-1-carboxylate which was used directly in the next step. LC-MS 509.3 [M+H]+, RT 1.28 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-91812fead42e49229427243386788226
Source noteuspto-grants-2016_08