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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014397Generated: October 30, 2026

HCID 59441760, compound → HCID 59441624, compound

https://huagongshe.com/reaction/1014397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59441760HCID 59441760—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59441624HCID 5944162493%

Reaction Steps

10% palladium on carbon (0.25 g, 8.52 mmol) was placed under N2 atm. MeOH (10 mL) was added, followed by a solution of N,N-dimethyl-2-[(2R)-2-methyl-5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-2-oxoethanamine (2.92 g, 9.96 mmol) in MeOH (190 mL). The slurry was purged with N2, then was placed under H2 atm via a rubber balloon and maintained at rt for 2 days. The resulting mixture was filtered through a pad of Celite and the filtrate was concentrated. The oily residue was taken up into Et2O and concentrated again to obtain (2R)-1-[(dimethylamino)acetyl]-2-methyl-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine as a beige solid (2.43 g, 93%). 1H NMR (400 MHz, DMSO-d8) δ ppm 1.17 (d, J=5.86 Hz, 3H), 2.26 (s, 6H), 2.44 (d, J=14.83 Hz, 1H), 3.02 (d, J=14.28 Hz, 1H), 3.10-3.27 (m, 1H), 3.36 (d, J=14.28 Hz, 1H), 3.72 (s, 3H), 4.52-4.77 (m, 3H), 6.72 (s, 1H), 7.48 (s, 1H); ESIMS (M+H)+=264.23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-4587e511c2d04435bba5c13f219ec731
Source noteuspto-grants-2011_07