Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736932Generated: October 30, 2026

Dimethylformamide → HCID 68591547, compound

https://huagongshe.com/reaction/736932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Piperidin-4-yl)-4,5-dihydro-1H-benzo[d][1,3]diazepin-2(3H)-oneHCID 11379587—
ReactantHCID 68591454HCID 68591454—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68591547HCID 68591547—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.8 g (11.0 mmol) CDT were added to a solution of 3.2 g (10.2 mmol) of ethyl (R)-2-amino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-propionate and 1.8 mL (10.3 mmol) ethyldiisopropylamine in 150 mL THF cooled to 0° C. and the reaction mixture was stirred for 45 min at this temperature and after removal of the ice bath stirred for a further 30 min. Then 2.5 g (10.2 mmol) 3-piperidin-4-yl-1,3,4,5-tetrahydro-1,3-benzodiazepin-2-one suspended in 50 mL THF were added. 40 mL DMF were added to the reaction solution and this was stirred for 2 h at 80° C. It was evaporated down i.vac., combined with 200 mL EtOAc and 200 mL 10% citric acid solution, the organic phase was separated off, extracted with 150 mL NaHCO3 solution and dried over Na2SO4. After elimination of the desiccant and solvent the desired product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595312B2
Source datasetuspto-grants-2009_09
ORD IDord-62e6d74260734c91b97dbebf82fe58a7
Source noteuspto-grants-2009_09