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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453902Generated: October 30, 2026

[(S)-1-Methyl-2-(7-{[(pyridine-3-carbonyl)-amino]-methyl}-furo[2,3-g]indazol-1-yl)-ethyl]-carbamic acid benzyl ester → N-[1-((S)-2-Aminopropyl)-1H-furo[2,3-g]indazol-7-ylmethyl]-nicotinamide

https://huagongshe.com/reaction/1453902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(S)-1-Methyl-2-(7-{[(pyridine-3-carbonyl)-amino]-methyl}-furo[2,3-g]indazol-1-yl)-ethyl]-carbamic acid benzyl esterHCID 68857650—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-[1-((S)-2-Aminopropyl)-1H-furo[2,3-g]indazol-7-ylmethyl]-nicotinamideHCID 6885607487%

Reaction Steps

To a solution of the product from Step C (0.16 g, 0.33 mmol) in methanol (20 mL) was added 10% Palladium on carbon (20 mg) and this mixture was stirred under an atmosphere of hydrogen at room temperature for two days. The reaction mixture was filtered and the filtrate evaporated to give a colorless oil (0.10 g, 87%): LC/MS m/z 350 [M+H]+; 1H NMR (CD3OD) δ 9.052 (s, 1H), 8.70 (m, 1H), 8.31 (m, 1H), 8.08 (s, 1H), 7.62 and 7.36 (ABq, J=9 Hz, 2H), 7.56 (m, 1H), 4.50 (overlapping m and s, 4H), 3.47 (m, 1H), 1.08 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476687B2
Source datasetuspto-grants-2009_01
ORD IDord-03855397ac06412193c0f90371ca12c1
Source noteuspto-grants-2009_01