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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420620Generated: November 2, 2026

Triethylamine → HCID 18612764, compound

https://huagongshe.com/reaction/1420620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dimethoxybenzoyl chlorideHCID 2734719—
ReactantHCID 18612788HCID 18612788—
SolventDichloromethaneHCID 6344—
ProductHCID 18612764HCID 1861276469.5%

Reaction Steps

To a cooled (0° C.) solution of 1.0 g (2.66 mmol) of 4-(4-methoxybenzenesulfonyl)-2,3,4,5-tetrahydro-1H-[1,4]benzodiazepine-3-carboxylate from Reference Example 12 and 1.85 ml (13.3 mmol) of triethylarnine in 8 ml of CH2Cl2 was added 1.17 g (6.65 mmol) of 2,4-dimethoxybenzoyl chloride. The mixture was stirred at room temperature overnight, diluted with CH2Cl2 and washed with 2N citric acid. The organic layer was washed with H2O, 1N Na2CO3, brine and dried over Na2SO4. The solvent was removed and the residue was chromatographed on thick layer silica gel plates with ethyl acetate-hexane (1:1) as an eluent to give 1.0 g of methyl 1-(2,4-dimethoxybenzoyl)-4-(4-methoxybenzenesulfonyl)-2,3,4,5-tetrahydro-1H-[1,4]benzodiazepine-3-carboxylate as a white foam. Anal. for C27H28H2O8S: Calc'd: C,60.0; H,5.2; N,5.2; Found: C,60.0; H,5.2; N,5.1; Mass Spectrum (ES): 541.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071903
Source datasetuspto-grants-2000_06
ORD IDord-f0f4526d51934e8aaaef11e4b1cf44f1
Source noteuspto-grants-2000_06