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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560857Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 178485330, compound

https://huagongshe.com/reaction/560857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
Reactant1-(5-Acetyl-4-methylthiazol-2-yl)-3-(4-(piperidine-1-carbonyl)benzyl)imidazolidin-2-oneHCID 58031385—
Reactant3-((3-(5-acetyl-4-methylthiazol-2-yl)-2-oxoimidazolidin-1-yl)methyl)-N-methylbenzamideHCID 58031394—
ProductHCID 178485330HCID 17848533054%

Reaction Steps

Following the procedure as described in Example 40, making variations as required to replace 1-(5-acetyl-4-methylthiazol-2-yl)-3-(4-(piperidine-1-carbonyl)benzyl)imidazolidin-2-one with 3-((3-(5-acetyl-4-methylthiazol-2-yl)-2-oxoimidazolidin-1-yl)methyl)-N-methylbenzamide to react with N,N-dimethylacetamide dimethyl acetal and further with hydrazine monohydrate, the title compound was obtained as a colorless solid in 54% yield: nip 259-261° C. (ethyl acetate); 1H NMR (300 MHz, DMSO-d6) δ 7.73-7.62 (m, 2H), 7.42-7.34 (m, 2H), 6.32 (br s, 1H), 4.51 (s, 2H), 4.13-4.04 (m, 2H), 3.49-3.41 (m, 2H), 2.97 (d, J=4.8 Hz, 3H), 2.60 (s, 3 H), 2.45 (s, 3H); MS (ES+) m/z 373.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063084B2
Source datasetuspto-grants-2011_11
ORD IDord-d6428f1dba9b48a088de1e959e0a6784
Source noteuspto-grants-2011_11