HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190331Generated: October 29, 2026
Lithium hydroxide, monohydrate → HCID 25175140, compound
https://huagongshe.com/reaction/2190331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | HCID 86628123 | HCID 86628123 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 25175140 | HCID 25175140 | — |
Reaction Steps
To a solution of methyl 3-(3-(benzo[d]thiazol-2-yl)-1-(3,3-diphenylpropyl)ureido)cyclopentanecarboxylate 35 (308 mg, 600 μmol) in 10:1 MeOH/H2O (5.5 ml) was added lithium hydroxide hydrate (50.3 mg, 1199 μmol). The reaction mixture was stirred for overnight at 55° C. Volatiles were removed by concentration under reduced pressure. The leftover residue was solubilized with 60 mL of a 1:1 mixture of Water and Ethyl Acetate. An additional 2 mL of 2M KOH was added. The organic phase was separated and the aqueous phase was extracted further with ethyl acetate (2×20 mL). The organic extracts were discarded and the aqueous layer was acidified with 10 mL of 10% aqueous HCl and extracted with ethyl acetate (3×20 mL). The combined organic extracts were dried with magnesium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica using 10->45% EtOAc/Hexanes as eluant to afford 36 as a white solid. LCMS (ES) calcd for C29H29N3O3S 499.2 found 500.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324396B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b4f9e266ead2492d96cdc922f5c049ec |
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| Source note | uspto-grants-2012_12 |
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