Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633853Generated: October 31, 2026

1,2-Dichloroethane → 1,4-Benzodiazepine deriv. 2

https://huagongshe.com/reaction/1633853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2R)-2-[(carbomethoxy)methyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-7-carboxylic acidHCID 11220043—
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1,4-Benzodiazepine deriv. 2HCID 653988292%

Reaction Steps

To a solution of (2R)-2-[(carbomethoxy)methyl]-4-methyl-3-oxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-7-carboxylic acid (0.4 g, 1.37 mmole) in dry DMF (10 mL) at RT was added 1-methyl-2-(methylaminomethyl)indole (0.26 g, 1.50 mmole), HOBt (0.20 g, 1.50 mmole), i-Pr2NEt (0.19 g, 1.50 mmole) and EDC (0.29 g, 1.50 mmole). After 18 hr the reaction solution was diluted with H2O (25 mL) and extracted with EtOAc (2×50 mL). The organic fractions were combined, washed sequentially with H2O and brine, then were dried (Na2SO4). Concentration under vacuum followed by chromatography on silica gel (95:5 CHCl3/MeOH) provided the title compound (0.56 g, 92%) as an off-white solid: MS (ES) m/e 449 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503903B1
Source datasetuspto-grants-2003_01
ORD IDord-2b5a0371449949ff9a8fab6b1f9b4017
Source noteuspto-grants-2003_01