HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897814Generated: October 30, 2026
trans-2-Phenyl-1-cyclopropanecarbonyl chloride → HCID 90693417, compound
https://huagongshe.com/reaction/897814
Participants
| Role | Name | HCID | Charge |
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| Reactant | trans-2-Phenyl-1-cyclopropanecarbonyl chloride | HCID 13656 | — |
| Reactant | tert-butyl 4-{[4-amino-3-(4-amino-3-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-4-hydroxy-1-piperidinecarboxylate | HCID 22347381 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 90693417 | HCID 90693417 | 76.5% |
Reaction Steps
To a mixture of tert-butyl 4-{[4-amino-3-(4-amino-3-methoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-4-hydroxy-1-piperidinecarboxylate (0.08 g, 0.00017 mol) in pyridine (4 mL) was added trans-2-phenyl-cyclopropane carbonyl chloride (0.035 g, 0.00019 mol) at −5° C. The mixture was stirred at −5° C. for 10 minutes then warmed up to room temperature to stir for 1 hours. The mixture was quenched with an aqueous 1N solution of sodium hydroxide. Pyridine was removed under reduced pressure. The residue was partitioned between water and dichloromethane (50 mL). The organic layer was washed with water. The solvents were removed under reduced and the residue was purified by RP-HPLC (Hypersilprep HS C18, 8 μm, 250×21.1 mm; 5%-100% over 35 min with 0.1 M ammonium acetate, 21 mL/min) to yield trans tert-butyl 4-{[4-amino-3-(3-methoxy-4-{[(2-phenylcyclopropyl)carbonyl]amino}phenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-4-hydroxy-1-piperidinecarboxylate (0.08 g, 0.00013 mol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-e5e56f4f4c01453ba89a48128051f40f |
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| Source note | uspto-grants-2005_07 |
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