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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620567Generated: October 30, 2026

1,2-Dichloroethane → HCID 14208219, compound

https://huagongshe.com/reaction/620567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantTriethylamineHCID 8471—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
Reactant3-Amino-5-phenyl-1,3-dihydro-1,4-benzodiazepin-2-oneHCID 4259649—
SolventDimethylformamideHCID 6228—
ProductHCID 14208219HCID 14208219—

Reaction Steps

3-(RS)-Amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one (1.3 g, 5.17 mmole), Boc-L-Phenylalanine (1.37 g, 5.17 mmole), HBT (0.70 g, 5.17 mmole), and EDC (0.99 g, 5.17 mmole) were combined in DMF (30 ml) and stirred at room temperature. The pH of the mixture was adjusted to 9.5 with triethylamine. After 1/2 hour, the DMF was removed in vacuo and the residue treated with 10% citric acid (10 ml), neutralized with NaCO3 and extracted with CH2Cl2 (3×15 ml). The combined organic layers were washed with water, dried over Na2CO3 filtered, and evaporated to dryness in vacuo. The residue was chromatographed on silica gel (90/3/0.3/0.3 CH2Cl2 /MeOH/H2 /HOAc) and the combined product fractions evaporated to dryness in vacuo. The residue was dissolved in CH2Cl2 (10 ml), washed with saturated Na2CO3 solution (2 ml), dried over Na2SO4, filtered and evaporated to dryness. The residue was treated with Et2O and evaporated five times to give the title compound as a mixture of diastereomers (m.p. 143°-153° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820834
Source datasetuspto-grants-1989_04
ORD IDord-ab5c75edc1034b7586264975f8e28536
Source noteuspto-grants-1989_04