HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510469Generated: October 26, 2026
Diisopropylethylamine → HCID 89561586, compound
https://huagongshe.com/reaction/510469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | N-(2-Amino-4,6-dichloropyrimidin-5-yl)formamide | HCID 10198177 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 89561586 | HCID 89561586 | 100% |
Reaction Steps
To a suspension of N-(2-amino-4,6-dichloropyrimidin-5-yl)formamide (10.0 g, 48.3 mmol) in 1,4-dioxane (400 mL) were added N,N-diisopropylethylamine (12.7 mL, 72.5 mmol) and piperazine-1-carboxylic acid tert-butyl ester (9.8 g, 53.1 mmol). The mixture was stirred at 55° C. for 1 h. The solvent was removed in vacuo and the residue was partitioned between DCM and water. The aqueous phase was extracted with further DCM and the combined organic fractions were washed with brine, then dried (Na2SO4) and evaporated in vacuo to give the title compound (17.1 g, 100%) as a white solid. LCMS (ES+) 357.4 (M+H)+, RT 1.08 minutes (method 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096614B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-50144f96d0134c90aa3a2851be357580 |
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| Source note | uspto-grants-2015_08 |
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