HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646761Generated: November 1, 2026
tert-butyl (3S)-3-aminopiperidine-1-carboxylate → HCID 58710594, compound
https://huagongshe.com/reaction/646761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl (3S)-3-aminopiperidine-1-carboxylate | HCID 1501975 | — |
| Reactant | HCID 68650629 | HCID 68650629 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58710594 | HCID 58710594 | 58.7% |
Reaction Steps
A mixture of 3-amino-6-{3-[(2-hydroxy-indan-1-ylamino)-methyl]-phenyl}-pyrazine-2-carboxylic acid methyl ester (400.0 mg, 1.02 mmol) and 1,1-dimethylethyl (3S)-3-aminopiperidine-1-carboxylate (970.0 mg, 4.84 mmol) was heated to 120° C. overnight. The reaction mixture was poured into water (100 mL), and extracted with ethyl acetate (2×50 mL) then dried over anhydrous sodium sulfate and filteration, concentration and purified by column chromatography (3% MeOH/Dichloromethane) and subsequently it was treated with 4.0 M HCl in dioxane (20 mL) to give 3-amino-6-[3-({[(1R,2S)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]amino}methyl)phenyl]-N-[(3S)-piperidin-3-yl]pyrazine-2-carboxamide, 275.0 mg (58.7% yield). 1H NMR (400 MHz, d4-MeOH): δ 8.72 (s, 2H), 8.18 (s, 1H), 7.80 (d, 1H), 7.60 (m, 2H), 7.38 (m, 3H), 4.80 (s, 1H), 4.50(s, 2H), 4.40 (m, 1H), 3.65 (m, 2H), 3.42 (m, 5H), 3.16 (m, 2H), 2.15 (m, 2H), 1.87 (m, 1H); MS (EI) for C26H30N6O2: 459.31 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07704995B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-3e195acc95824f08ae1dd7ccc873ea98 |
|---|
| Source note | uspto-grants-2010_04 |
|---|