Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343230Generated: October 31, 2026

3-[1-(tert-Butyl-phenyl-carbamoylmethyl)-2,4-dioxo-5-phenyl-2,3,4,5,-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylmethyl]-indazole-1-carboxylic acid tert-butyl ester → HCID 178449516, compound

https://huagongshe.com/reaction/343230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[1-(tert-Butyl-phenyl-carbamoylmethyl)-2,4-dioxo-5-phenyl-2,3,4,5,-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylmethyl]-indazole-1-carboxylic acid tert-butyl esterHCID 67696819—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178449516HCID 17844951657.7%

Reaction Steps

263 mg (0.392 mmol) 3-[1-(tert-Butyl-phenyl-carbamoylmethyl)-2,4-dioxo-5-phenyl-2,3,4,5,-tetrahydro-1H-benzo[b][1,4]diazepin-3-ylmethyl]-indazole-1-carboxylic acid tert-butyl ester, prepared as in Intermediate 65, is dissolved in 3 mL 4N HCl in Dioxane and stirred 1 h at ambient temperature. The solvent is removed in vacuo and the residue taken into EtOAc (50 mL), washed with satd. NaHCO3 (30 mL) and brine (30 mL), dried (MgSO4), filtered and concentrated in vacuo. The crude product is purified by flash chromatography on 5 g silica gel eluted successively with EtOAc/Hexanes (1:2, 50 mL), (2:3, 80 mL), (1:1, 50 mL). Appropriate fractions were combined and concentrated in vacuo to give 65 mg (0.113 mmol) of the title compound as a white foam: 1H NMR (CDCl3, 300 MHz) δ7.82 (d, 1H, J=7.5), 7.43-7.06 (m, 16H), 4.19 (m, 2H), 4.08 (m, 1H), 3.79 (m, 1H), 3.63 (m, 1H), 1.37 (s, 9H); low resolution MS (FAB) m/e 572.2 (MH+); TLC Rf =0.41 (EtOAc/Hexanes, 3:2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859007
Source datasetuspto-grants-1999_01
ORD IDord-fb26bcd9c7444e11955fb937f7e54c8c
Source noteuspto-grants-1999_01