HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270205Generated: October 31, 2026
Diisopropylethylamine → HCID 86591333, compound
https://huagongshe.com/reaction/1270205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | HCID 18449305 | HCID 18449305 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86591333 | HCID 86591333 | 99.9% |
Reaction Steps
Boc-piperazine (122 mg, 0.65 mmol) was added to the solution of (2-Chloro-pyrido[2,3-d]pyrimidin-4-yl)-(2,4-dichloro-benzyl)-amine(185 mg, 0.54 mmol) and N,N-diisopropylethylamine (145 μL, 0.82 mmol) in n-butanol (2 mL). The reaction mixture was stirred at 85° for 10 h. All starting material was consumed as seen on HPLC. The reaction mixture was concentrated at room temperature under vacuo. The resulting residue was suspended in 2 mL of TFA-CH2Cl2 (1:1) mixture and stirred at room temperature for 45 minutes. The reaction mixture was concentrated in vacuo, diluted with saturated aqueous sodium bicarbonate solution. The aqueous layer was extracted with CH2Cl2 (2×10 mL), dried (Na2SO4) and concentratd to furnish (2,4-Dichloro-benzyl)-(2-piperazin-1-yl-pyrido[2,3-d]pyrimidin-4-yl)-amine(210 mg) as pale brown oil. The crude was carried forward as such in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202249B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-5c3a8ee0e53d4ab3b34140ede3ebd062 |
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| Source note | uspto-grants-2007_04 |
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