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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816452Generated: November 2, 2026

Ethyl Acetate → (11aS)-1,2,3,10,11,11a-Hexahydro-7-methoxy-8-[3-[[(11aS)-2,3,5,11a-tetrahydro-7-methoxy-5-oxo-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl]oxy]propoxy]-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one

https://huagongshe.com/reaction/1816452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCalcium CarbonateHCID 10112—
ReactantAcetonitrile--water (1/1)HCID 18373917—
ReactantHCID 86594410HCID 86594410—
CatalystMercuric ChlorideHCID 24085—
Product(11aS)-1,2,3,10,11,11a-Hexahydro-7-methoxy-8-[3-[[(11aS)-2,3,5,11a-tetrahydro-7-methoxy-5-oxo-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl]oxy]propoxy]-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-oneHCID 406087—

Reaction Steps

A solution of the (2S)-N-{4-[3-(7-Methoxy-(2R)-hydroxy-(11aS)-1,2,3,10,11,11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-5-one-8-yloxy)propoxy]-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal IV (674 mg, 1 mmol), HgCl2 (794 mg, 2.93 mmol) and CaCO3 (300 mg, 3 mmol) in CH3CN/H2O (4:1, 15 mL) was stirred at room temperature for 12 h until TLC (EtOAc), indicates complete loss of starting material. Then organic layer is evaporated in vacuum and the residue is diluted with EtOAc. To this saturated NaHCO3 was added slowly at room temperature and the mixture is filtered through celite and washed with ethylacetate. The filterate is evaporated in vacuum to get crude 7-Methoxy-8-{3-[7-methoxy-(11aS)-1,2,3,10,11,11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-5-one-8-yloxy]propoxy}-(11aS)-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine-5-one of formula V, which was further purified by column chromatography on silica gel eluting with methanol:EtOAc (3:7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884799B2
Source datasetuspto-grants-2005_04
ORD IDord-fc245bc1aca34dc3b1469e3cc23f2825
Source noteuspto-grants-2005_04