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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786122Generated: November 2, 2026

N-{[(5R)-16-(Dimethylamino)-4-oxo-2,3,15,17,18-pentaazabicyclo[12.3.1]octadeca-1(18),10,14,16-tetraen-5-yl]methyl}-N-benzoxyformamide → N-{[(5R)-16-(Dimethylamino)4-oxo-2,3,15,17,18-pentaazabicyclo[12.3.1]octadeca-1(18),14,16-trien-5-yl]methyl}-N-hydroxyformamide

https://huagongshe.com/reaction/1786122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-{[(5R)-16-(Dimethylamino)-4-oxo-2,3,15,17,18-pentaazabicyclo[12.3.1]octadeca-1(18),10,14,16-tetraen-5-yl]methyl}-N-benzoxyformamideHCID 86621284—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-{[(5R)-16-(Dimethylamino)4-oxo-2,3,15,17,18-pentaazabicyclo[12.3.1]octadeca-1(18),14,16-trien-5-yl]methyl}-N-hydroxyformamideHCID 11372389—

Reaction Steps

To a solution of N-{[(5R)-16-(dimethylamino)-4-oxo-2,3,15,17,18-pentaazabicyclo[12.3.1]octadeca-1(18),10,14,16-tetraen-5-yl]methyl}-N-benzoxyformamide (75 mg) in MeOH (15 mL) was added 10% Pd/C (15 mg, 20% w/w). The reaction mixture was subjected to hydrogenation for 3 hours at room temperature. The reaction mixture was then filtered through a pad of Celite, and washed with MeOH (10 mL×2). Removal of the solvent provided the title compound. MH+380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507726B2
Source datasetuspto-grants-2009_03
ORD IDord-7f785d9910ca43b9bfc8a79f71909a1e
Source noteuspto-grants-2009_03