HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205593Generated: October 26, 2026
tert-Butyl piperazine-1-carboxylate → HCID 118207781, compound
https://huagongshe.com/reaction/2205593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | (S)-1-(6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)ethanamine | HCID 86707977 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 118207781 | HCID 118207781 | 40% |
Reaction Steps
To a 50 mL pear flask were added tert-butyl piperazine-1-carboxylate (2.44 g, 12.7 mmol) and (S)-1-(6-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridin-5-yl)ethanamine (1.54 g, 6.06 mmol) in 1,4-dioxane (15 mL). To this solution was added potassium 2-methylpropan-2-olate (1 M in THF) (13.3 mL, 13.3 mmol), and the resulting mixture was heated to 90° C. for 45 minutes. After cooling for 10 minutes, the red mixture was poured into saturated NaHCO3 (300 mL) and then extracted with EtOAc (3×). The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo to give crude product, which was purified by preparative HPLC (acid mode, 25-65% ACN/water gradient). The product-containing fractions were combined, concentrated in vacuo, and then partitioned between saturated NaHCO3 and EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated to give the title compound (872 mg, 40.0%). ESI-MS m/z [M+H]+ calc'd for C19H29N5O2, 360. found 360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371321B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-e7b18ddbcdf643ccb8dfbd4800a2a005 |
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| Source note | uspto-grants-2016_06 |
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