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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427230Generated: November 3, 2026

methyl 2-(4-(tert-butoxycarbonylamino)-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoate → methyl 2-(4-amino-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoate

https://huagongshe.com/reaction/1427230

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 2-(4-(tert-butoxycarbonylamino)-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoateHCID 70562967—
SolventHydrochloride methanolHCID 21893726—
Productmethyl 2-(4-amino-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoateHCID 70561351—

Reaction Steps

A mixture of methyl 2-(4-(tert-butoxycarbonylamino)-1H-indazol-1-yl)-2-(4-chlorophenyl)butanoate (3.0 g, 6.8 mmol), as described in Example 18 Step D, in 4 N HCl/MeOH (20 mL) was stirred at room temperature for 2 h. After removing the solvent, the residue was dissolved in ethyl acetate (80 mL), pH value adjusted to 9-10 with saturated sodium bicarbonate solution, dried over sodium sulfate, then filtered. After removing the organic solvent, the residue was used for the next step without purification. LC/MS m/z=344.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933113B2
Source datasetuspto-grants-2015_01
ORD IDord-e065240689d4441986da8b415d686027
Source noteuspto-grants-2015_01