HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754414Generated: October 28, 2026
p-Toluenesulfonic acid monohydrate → HCID 71811349, compound
https://huagongshe.com/reaction/1754414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 58287145 | HCID 58287145 | — |
| Reactant | HCID 81629389 | HCID 81629389 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 71811349 | HCID 71811349 | 47% |
Reaction Steps
A mixture of N-(2-chloro-5-fluoropyrimidin-4-yl)octahydroindolizin-7-amine (54 mg, 0.2 mmol), 1-(5-amino-2-cyclopropyl-4-fluorophenyl)-4-methyl-1H-tetrazol-5-one (52 mg, 0.21 mmol; prepared according to US20110130415 pages 43-48, which is hereby incorporated by reference in its entirety) and para-toluenesulfonic acid monohydrate (38 mg, 0.2 mmol) in isopropyl alcohol (3 ml) were combined in a sealed vial, heated to 70° C. and stirred for 2 days. After cooling, the mixture was concentrated under vacuum to leave a crude residue. The residue was purified by preparative high-performance liquid chromatography to give a solid. The solid was partitioned between EtOAc (20 ml) and 1N NaOH (20 ml). The aqueous layer was extracted with EtOAc (2×20 ml) and the combined organic extracts were dried (MgSO4), filtered and the solvent removed in vacuo to leave the product (46 mg, 47%) as a solid after freeze-drying from MeCN/H2O.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169249B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-26cd10c919cd4a28a914b79536973db8 |
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| Source note | uspto-grants-2015_10 |
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