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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206646Generated: November 1, 2026

HCID 117778962, compound → HCID 117779063, compound

https://huagongshe.com/reaction/2206646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 117778962HCID 117778962—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 117779063HCID 11777906375%

Reaction Steps

A mixture of compound ethyl 7-(1-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)-2-chloro-6-methyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate (75 mg, 0.16 mmol) and Pd/C (10 mg) in methanol (10 mL) was stirred under 50 psi of hydrogen at room temperature overnight. The reaction mixture was filtered and the filtrate was concentrated to give product ethyl 7-(1-(1-(tert-butoxycarbonyl)piperidin-4-yl)ethyl)-6-methyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate (50 mg, yield: 72%). LRMS (M+H+) m/z: calcd 450.2. found 451.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-575a4c0a02cb4b56a59fe05c6a545ec8
Source noteuspto-grants-2016_06