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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
ReactantHCID 68650629HCID 68650629—
SolventWaterHCID 962—
ProductHCID 58710594HCID 5871059458.7%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-3e195acc95824f08ae1dd7ccc873ea98
Source noteuspto-grants-2010_04