HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467349Generated: November 1, 2026
Diisopropylethylamine → HCID 70652638, compound
https://huagongshe.com/reaction/1467349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (3R)-3-Aminopiperidine, 3-BOC protected | HCID 1514172 | — |
| Reactant | HCID 86681288 | HCID 86681288 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70652638 | HCID 70652638 | — |
| Product | HCID 86681289 | HCID 86681289 | — |
Reaction Steps
tert-Butyl (3R)-piperidin-3-ylcarbamate (0.234 g, 1.168 mmol), methyl bromo(2,6-difluorophenyl)acetate (0.434 g, 1.636 mmol) and DIPEA (0.612 mL, 3.51 mmol) were taken up in MeCN (11 mL) in a 20 mL microwave vial. The reaction was stirred at 90° C. for 18 hours. Room temperature was attained, and the solvent removed in vacuo. Purification of the residue by MPLC (6-50% EtOAc-hexanes) gave (S)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)-acetate as a yellow gum and (R)-methyl 2-((R)-3-(tert-butoxycarbonylamino)piperidin-1-yl)-2-(2,6-difluorophenyl)acetate as a yellow gum (R,R).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999957B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-35184d8caff04238b7577466b440eb6f |
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| Source note | uspto-grants-2015_04 |
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