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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808791Generated: November 2, 2026

Methanol → HCID 52180852, compound

https://huagongshe.com/reaction/1808791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,4-DioxaneHCID 31275—
Reactanttert-Butyl [(2S)-1-(azetidin-1-yl)-3-methyl-1-oxobutan-2-yl]carbamateHCID 52180842—
SolventHydrochloric AcidHCID 313—
ProductHCID 52180852HCID 5218085273.2%

Reaction Steps

(S)-Tert-butyl 1-(azetidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamate (Compound D) (23.56 g, 90.07 mmol) was stirred in 4M HCl in dioxane (56.3 mL, 225 mmol) for 30 min. Additional dioxane and MeOH was added until the reaction mixture became a clear solution. The solvent was removed under reduced pressure and conc. HCl (3.00 mL, 30.4 mmol) was added. The mixture was stirred for 5 h before the solvent was removed. The residue was purified via Biotage (gradient; EtOAc:MeOH (2% TEA), 99:1 to 90:10, then EtOAc:MeOH (2% TEA) 90:10 to 0/100 KP-SIL 340 g. The solvent was removed under reduced pressure to give the title compound (10.3 g, 70.3%). 1H NMR (600 MHz, CH3OD) δ 1.03, 1.06, 2.07-2.16, 2.33-2.41, 3.71, 3.99-4.07, 4.07-4.14, 4.25-4.33, 4.33-4.41. Total no of protons: 14. LCMS (M+H)+: 157.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361998B2
Source datasetuspto-grants-2013_01
ORD IDord-0e50734ca9494ec0b771495786ae106d
Source noteuspto-grants-2013_01