Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297101Generated: October 29, 2026

Dichloromethane → 7,8-dimethoxy-1-methyl-5-(2-phenylethyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/1297101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant7,8-Dimethoxy-1-methyl-5-(2-phenylethynyl)-1,3-dihydro-1,4-benzodiazepin-2-oneHCID 57397361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product7,8-dimethoxy-1-methyl-5-(2-phenylethyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-oneHCID 99458025%

Reaction Steps

Stir a mixture of 80 mg (0.24 mmol) of 7,8-dimethoxy-1-methyl-5-(2-phenylethynyl)-1,3-dihydro-1,4-benzodiazepin-2-one 132, 15 mg of 10% Pd/C by weight in 5 ml of MeOH and 5 ml of CH2Cl2 under 70 psi of H2 for 48 hours. Filter the suspension on celite, rinse three times with 10 ml of MeOH. Evaporate to dryness and purify by silica chromatography (AcOEt 1/hexane 1, then AcOEt). Yield: 5%. M: 112–115° C. 1H-NMR (CDCl3, 300 MHz): d 2.95–3.07 (m, 4H, CH2CH2), 3.28 (s, 3H, NCH3), 3.87 (s, 3H, OCH3), 3.93 (s, 3H, OCH3), 4.10 (AB system, ? d=0.96, JAB=10.2, 2H, CH2), 6.67 (s, 1H Ar), 6.78 (s, 1H Ar), 7.15–7.25 (m, 5H Ar). Mass: (M+H)+=339.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250410B2
Source datasetuspto-grants-2007_07
ORD IDord-840ffd72c84b4141bc21d96edcb2874c
Source noteuspto-grants-2007_07