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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666767Generated: October 31, 2026

Isopropanol hydrochloride → HCID 24765038, compound

https://huagongshe.com/reaction/1666767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanol hydrochlorideHCID 21912024—
ReactantHCID 57552289HCID 57552289—
SolventEthanolHCID 702—
ProductHCID 24765038HCID 2476503891%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044083B2
Source datasetuspto-grants-2011_10
ORD IDord-399a9f0b0b634a5fb824c5baade2e2ce
Source noteuspto-grants-2011_10