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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423108Generated: November 3, 2026

1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate → (S)-5-(3-benzylpiperazin-1-yl)-3-cyclobutyl-1-methyl-1H-indazole

https://huagongshe.com/reaction/1423108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylateHCID 17750441—
Reactant5-Bromo-3-cyclobutyl-1-methyl-1H-indazoleHCID 58188999—
Product(S)-5-(3-benzylpiperazin-1-yl)-3-cyclobutyl-1-methyl-1H-indazoleHCID 5818916899%

Reaction Steps

The title compound was prepared by the method outlined for Example 1 using 5-Bromo-3-cyclobutyl-1-methyl-1H-indazole as the aryl halide and (S)-2-benzyl-piperazine-1-carboxylic acid tert-butyl ester as the amine component to afford the title compound as a brown oil (409 mg, 99%). 1H NMR (MeOH-d4) 8.72 (d, J=8.7 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.32-7.18 (m, 6H), 4.08 (s, 3H), 3.79-3.46 (m, 3H), 3.35-3.34 (m, 1H), 3.31-3.30 (m, 2H), 3.15-3.07 (m, 4H), 2.88-2.77 (m, 5H), 2.69-2.61 (m, 1H). LC/MS (Method B) 2.49 min, [M+1]+ 361.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927546B2
Source datasetuspto-grants-2015_01
ORD IDord-e16e87e0e4524d32aaaa33b8d404daa4
Source noteuspto-grants-2015_01