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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830099Generated: November 2, 2026

Dimethylformamide → HCID 10282918, compound

https://huagongshe.com/reaction/1830099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
ReactantHCID 21947847HCID 21947847—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 10282918HCID 10282918—

Reaction Steps

The title compound was prepared in the manner of Example 19, Step A using 2,5-dimethoxy-2′-trifluoromethyl-[1,1′-biphenyl]-4-carboxylic acid of Step A (1.63 g, 5 mmol), oxalyl chloride (700 μL, 8 mmol), N,N-dimethylformamide (10 μL), 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine (0.93 g, 5 mmol) and Hünig's base (1.78 ml, 10 mmol). Flash chromatography over silica gel using a solvent gradient from 30% ethyl acetate in hexane to 100% ethyl acetate provided the title compound (0.900 g) as a solid. Recrystallization from acetone/hexane yielded white needles, m.p. 210–213° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064120B2
Source datasetuspto-grants-2006_06
ORD IDord-c0ab6cac998e4450939743a66ac8313d
Source noteuspto-grants-2006_06