Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73912Generated: October 25, 2026

Water → ({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/73912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantStannous chloride dihydrateHCID 61436—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl-({methyl-[2-(6-nitro-indol-1-yl)-2-oxo-ethyl]-carbamoyl}-methyl)-carbamic acid tert-butyl esterHCID 66675158—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl esterHCID 6667569699.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl-({methyl-[2-(6-nitro-indol-1-yl)-2-oxo-ethyl]-carbamoyl}-methyl)-carbamic acid tert-butyl ester (12.4 g, 30.6 mmol), SnCl2.2H2O (34.5 g, 153.2 mmol) and DIEA (74.8 mL, 429 mmol) in ethanol (112 mL) was heated to 70° C. for 3 h. Water and EtOAc were added and the mixture was filtered through a short plug of Celite. The organic layer was separated, dried over Na2SO4 and concentrated to yield ({[2-(6-Amino-indol-1-yl)-2-oxo-ethyl]-methyl-carbamoyl}-methyl)-methyl-carbamic acid tert-butyl ester (B-26) (11.4 g, quant.). HPLC ret. time 2.11 min, 10-99% CH3CN, 5 min run; ESI-MS 375.3 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-cb299e5a5c2a4a48bea4bfb1da60fa89
Source noteuspto-grants-2014_09