HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014330Generated: October 26, 2026
Nitrogen → 1-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-methyl-1-oxo-2-propanol
https://huagongshe.com/reaction/1014330
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | 2-methyl-1-[5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-1-oxo-2-propanol | HCID 59442126 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-methyl-1-oxo-2-propanol | HCID 59441738 | 93.2% |
Reaction Steps
A solution of 2-methyl-1-[5-(methyloxy)-6-nitro-2,3-dihydro-1H-indol-1-yl]-1-oxo-2-propanol (840 mg, 3.00 mmol) in ethyl acetate (100 mL) and Ethanol (50 mL) was degassed with N2 and to this was added 10% Pd/C (31.9 mg, 0.300 mmol). The reaction was maintained at 50 psi H2(g) overnight at rt on the Fisher-Porter apparatus. The catalyst was removed by vacuum filtration, rinsed with ethyl acetate (200 mL), and the filtrate was concentrated under reduced pressure to provide 1-[6-amino-5-(methyloxy)-2,3-dihydro-1H-indol-1-yl]-2-methyl-1-oxo-2-propanol (0.7 g, 93%). ESIMS (M+H)+=251. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.36 (s, 6H) 2.91 (t, J=8.03 Hz, 2 H) 3.71 (s, 3 H) 4.31 (t, J=8.03 Hz, 2 H) 4.57 (s, 2 H) 5.36 (s, 1 H), 6.70 (s, 1 H) 7.57 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-f8700c0073124001afc3716ff0a88397 |
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| Source note | uspto-grants-2011_07 |
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