HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666767Generated: October 31, 2026
Isopropanol hydrochloride → HCID 24765038, compound
https://huagongshe.com/reaction/1666767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol hydrochloride | HCID 21912024 | — |
| Reactant | HCID 57552289 | HCID 57552289 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24765038 | HCID 24765038 | 91% |
Reaction Steps
A solution of di-tert-butyl 2-(5-(2-((3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido)methyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethyl phosphate (3.66 g, 4.89 mmol) in EtOH (0.2M, 24 mL) was treated with SN HCl/iPrOH (2.93 mL, 14.7 mmol) at room temperature. Stirring at room temperature was continued overnight. The solvent was evaporated in vacuo, and the residue was coevaporated from toluene, and ether (2×). The beige foam was taken in MeOH and poured slowly into a beaker containing water. The precipitated solids were collected by filtration to provide 2.83 g (91%) of the desired product. MS (APCI+) m/z 637 (M+1) was detected. 1H NMR (400 MHz, DMSO-d6) δ 8.30 (s, 1H), 8.00 (s, 1H), 7.71 (d, 1H, J=9 Hz), 6.88-7.37 (m, 10H), 6.24 (s, 1H), 4.61 (br, 1H), 4.28 (d, 2H, J=5.7 Hz), 4.19 (dd, 2H, J=5.2 Hz), 2.35 (s, 3H), 1.25 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044083B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-399a9f0b0b634a5fb824c5baade2e2ce |
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| Source note | uspto-grants-2011_10 |
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