HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507506Generated: November 3, 2026
Diisopropylethylamine → HCID 136504501, compound
https://huagongshe.com/reaction/1507506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-butyl (3R)-3-aminopiperidine-1-carboxylate | HCID 1501974 | — |
| Reactant | HCID 178525124 | HCID 178525124 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136504501 | HCID 136504501 | — |
Reaction Steps
A mixture of benzyl 4-[5-(1,3-benzothiazol-2-yl)-4-chloro-6-hydroxypyrimidin-2-yl]piperidine-1-carboxylate (48.1 mg, 0.10 mmol, 1.00 equiv), tert-butyl (3R)-3-aminopiperidine-1-carboxylate (20.1 mg, 0.10 mmol, 1.00 equiv), and N-ethyl-N-isopropylpropan-2-amine (25.4 mg, 0.20 mmol, 1.97 equiv) in ethanol (3 ml) was heated overnight at 90° C. in an oil bath. Upon concentrated under vacuum, the residue was purified by flash chromatography on a silica gel column eluting with petroleum ether/ethyl acetate (1:1) to afford the title compound. as a yellow solid. MS m/z [M+H]+ (ESI): 645.
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-eb4921d957464f0fa068841daacb00b1 |
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| Source note | uspto-grants-2015_12 |
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