HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507487Generated: October 30, 2026
tert-butyl (3R)-3-aminopiperidine-1-carboxylate → HCID 89554205, compound
https://huagongshe.com/reaction/1507487
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl (3R)-3-aminopiperidine-1-carboxylate | HCID 1501974 | — |
| Reactant | 4-Chloro-6-methoxy-2-(methylthio)pyrimidine | HCID 9836999 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 89554205 | HCID 89554205 | — |
Reaction Steps
Compound 2 (3.6 g, 18.9 mmol) and (R)-1-Boc-3-aminopiperidine (9.45 g, 47.2 mmol) were dissolved in ethanol (50 mL) and TEA (10.5 mL, 76 mmol) was added. The reaction was sealed and heated to 130° C. for 72 h. The orange solution was concentrated and the residue was purified by column chromatography on silica gel, eluting with EtOAc/hexane to give the title compound as a white foam. 1H NMR (CDCl3) δ 5.40 (s, 1H), 4.78 (br s, 1H), 3.88 (s, 3H), 3.84-3.81 (m, 1H), 3.58-3.56 (m, 2H), 3.17-3.05 (m, 2H), 2.49 (s, 3H), 2.04-1.91 (m, 1H), 1.75-1.67 (m, 1H), 1.57-1.51 (m, 2H), 1.44 (s, 9H); LCMS 2.30 min, 355 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221809B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-751662a0496e490db449d441138d17f9 |
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| Source note | uspto-grants-2015_12 |
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