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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396916Generated: November 2, 2026

1-Methylimidazole → 2-propen-1-yl (3S)-2-((2R)-3-cyclopentyl-2-{[formyl(tetrahydro-2H-pyran-2-yloxy)amino]methyl}propanoyl)-3-[(2-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylate

https://huagongshe.com/reaction/1396916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
Reactant2-AminopyrimidineHCID 7978—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-((2R)-3-cyclopentyl-2-{[formyl(tetrahydro-2H-pyran-2-yloxy)amino]methyl}propanoyl)-1-[(2-propen-1-yloxy)carbonyl]-3-pyrazolidinecarboxylic acidHCID 86706358—
SolventDimethylformamideHCID 6228—
Product2-propen-1-yl (3S)-2-((2R)-3-cyclopentyl-2-{[formyl(tetrahydro-2H-pyran-2-yloxy)amino]methyl}propanoyl)-3-[(2-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylateHCID 8670636024%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Methylimidazole (38.1 μl, 0.478 mmol) was added into the solution of 2-((2R)-3-cyclopentyl-2-{[formyl(tetrahydro-2H-pyran-2-yloxy)amino]methyl}propanoyl)-1-[(2-propen-1-yloxy)carbonyl]-3-pyrazolidinecarboxylic acid (115 mg, 0.239 mmol) in N,N-dimethylformamide (DMF) (1.6 ml). The resulting solution was cooled to 0° C., and then mesyl chloride (19.41 μl, 0.251 mmol) was added dropwise at 0° C. To the reaction mixture was added 2-pyrimidinamine (34.1 mg, 0.358 mmol). After stirring for 3.5 hrs at ambient temperature, the reaction solution was purified by RP-HPLC to yield 2-propen-1-yl (3S)-2-((2R)-3-cyclopentyl-2-{[formyl(tetrahydro-2H-pyran-2-yloxy)amino]methyl}propanoyl)-3-[(2-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylate (32 mg, 0.057 mmol, 24% yield). MS (ES+) m/z 559.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-edfb4fae7b574f0898346cb4be5ab767
Source noteuspto-grants-2014_12