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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816451Generated: October 30, 2026

Methanol → HCID 86594410, compound

https://huagongshe.com/reaction/1816451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantStannous chloride dihydrateHCID 61436—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86594409HCID 86594409—
SolventDichloromethaneHCID 6344—
ProductHCID 86594410HCID 86594410—

Reaction Steps

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-nitrobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal III (704 mg, 1.0 mmol) was dissolved in dichloromethane (5 mL), methanol (10 mL) and added SnCl2.2H2O (1.124 g, 5.0 mmol), was refluxed for 1.5 h. The reaction mixture was then carefully adjusted to pH 8 with saturated NaHCO3 solution and then extracted with ethyl acetate (3×20 mL). The combined organic phase was dried over Na2SO4 and evaporated under vacuum to afford the crude (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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884799B2
Source datasetuspto-grants-2005_04
ORD IDord-ce95bc53e70c43d1b222e6dc0703edd2
Source noteuspto-grants-2005_04