HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966396Generated: October 25, 2026
(4-aminophenyl)(4-methylpiperazin-1-yl)methanone → HCID 44183499, compound
https://huagongshe.com/reaction/1966396
Participants
| Role | Name | HCID | Charge |
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| Reactant | (4-aminophenyl)(4-methylpiperazin-1-yl)methanone | HCID 231408 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 2-Chloro-7-(3,5-difluoro-4-morpholin-4-ylmethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidine | HCID 86633271 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44183499 | HCID 44183499 | — |
Reaction Steps
In a sealed tube, 2-chloro-7-(3,5-difluoro-4-morpholin-4-ylmethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidine (50.0 mg, 0.130 mmol), (4-Amino-phenyl)-(4-methyl-piperazin-1-yl)-methanone (42.1 mg, 0.182 mmol), KOtBu (21.1 mg, 0.182 mmol) and SK-CC02-A (12.5 mg, 0.020 mmol, Pd catalyst 2-(Dimethylaminomethyl)-ferrocen-1-yl-palladium(II)-chlorid Dinorbornylphosphin Complex, Fluka No. 44696) are suspended in THF (2 ml) under Ar. The reaction mixture is stirred at 80° C. for 1.5 h, cooled to rt, and then filtered through a Celite plug. The filtrate is concentrated under reduce pressure. The residue is purified by reverse phase prep-HPLC (Waters) to afford the title compound (2) as a white solid. HPLC: tR=0.89 min (Method A); MS-ES: (M+H)+=548.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420657B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-eefa320a3b1d47929f59bb691e0228ff |
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| Source note | uspto-grants-2013_04 |
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