HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370948Generated: October 31, 2026
HCID 58065786, compound → HCID 56644723, compound
https://huagongshe.com/reaction/2370948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58065786 | HCID 58065786 | — |
| Reactant | HCID 58065809 | HCID 58065809 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 56644723 | HCID 56644723 | 50% |
Reaction Steps
A mixture of 4-(2,2,6,6-tetramethylpiperidin-4-ylamino)-2-chloropyrimidine-5-carboxamide (178 mg, 0.570 mmol, 1 equiv), 4-cyclopropyl-2-fluoro-5-(1H-tetrazol-1-yl)benzenamine (150 mg, 0.684 mmol, 1.2 equiv), and PTSA monohydrate (230 mg, 1.20 mmol, 2.1 equiv) in IPA (6 mL) were heated to 100° C. overnight giving a precipitate. The precipitate was collected by vacuum filtration and rinsed with IPA. The solid was taken in EtOAc then adjusted to ca. pH 12-14 with 1N NaOH. The aqueous and organic layers were partitioned. The aqueous layer was extracted with EtOAc (2×150 mL). The combined organics were washed with 1N NaOH (1×150 mL), dried (Na2SO4), filtered, and concentrated to give the desired product (128 mg, 50%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710223B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e5b7dbbe750f432d89e7df6efa3b158d |
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| Source note | uspto-grants-2014_04 |
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