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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389476Generated: October 30, 2026

tert-Butyl {2-[3-(2,3-dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetate → {2-[3-(2,3-Dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetic acid

https://huagongshe.com/reaction/2389476

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl {2-[3-(2,3-dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetateHCID 86620027—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product{2-[3-(2,3-Dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetic acidHCID 1151813113.2%

Reaction Steps

tert-Butyl {2-[3-(2,3-dihydro-1-ethyloxycarbonyl-3-oxo-indazol-2-yl)-propylsulfanyl]-benzoimidazol-1-yl}-acetate (Precursor G-01b, 63.8 mg, 0.1 mmol) is stirred in TFA/dichloromethane (1:1, 2 ml) at rt overnight. The solvents are removed in vacuo. The crude is taken up in chloroform (1 ml) and filtered over cotton wool. The solvent is removed in vacuuo and the residue is dried under high vacuum. This yields the title compound (6 mg) in 11% as a colourless oil: tR=2.24 min (LC-2), ESI-MS (pos.): m/z 455.11 [M+H]+, ESI-MS (neg.): m/z 453.22 [M−H]+; 1H-NMR (DMSO-d6): δ (ppm) 1.31 (t, 3H, CH3), 2.03 (quint., 2H, CH2CH2N), 3.18 (m, 2H, SCH2), 4.23 (t, 2H, CH2N), 4.36 (q, 2H, OCH2), 4.94 (s, 2H, CH2CO2), 7.10-7.15 (m, 2H, m), 7.39 (t, 1 Harom), 7.46 (m, 2Harom), 7.70-7.78 (m, 2Harom), 7.87 (d, 1Harom)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273740B2
Source datasetuspto-grants-2012_09
ORD IDord-2d662801880c46219aa0f0506e5eb83b
Source noteuspto-grants-2012_09