Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915760Generated: November 1, 2026

5-chloro-1-methyl-4-nitro-1H-pyrazole → (R)-tert-butyl 4-(4-amino-1-methyl-1H-pyrazol-5-yl)-3-ethylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1915760

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-chloro-1-methyl-4-nitro-1H-pyrazoleHCID 12344836—
Reactant(R)-1-Boc-3-EthylpiperazineHCID 24820337—
Product(R)-tert-butyl 4-(4-amino-1-methyl-1H-pyrazol-5-yl)-3-ethylpiperazine-1-carboxylateHCID 86679973—

Reaction Steps

Following the procedure for Intermediate 10 starting from 5-chloro-1-methyl-4-nitro-1H-pyrazole from Example 1 and (R)-tert-butyl 3-ethylpiperazine-1-carboxylate gave (R)-tert-butyl 4-(4-amino-1-methyl-1H-pyrazol-5-yl)-3-ethylpiperazine-1-carboxylate as an orange gum (118 mg, 67% over two steps). LCMS (ES+) m/z 310 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614206B2
Source datasetuspto-grants-2013_12
ORD IDord-16bf9659209141c695e17a2f989a4e4b
Source noteuspto-grants-2013_12