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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654793Generated: November 1, 2026

Dichloromethane → HCID 135710756, compound

https://huagongshe.com/reaction/1654793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 135710757HCID 135710757—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 135710756HCID 13571075668.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

0.21 g of 3methyl-5-(2-chlorophenyl)-8-(3-butynyloxycarbonyl)-6,7,8,9-tetrahydro-1H,3H-pyrido[4',3':4,5] thieno[3,2-f][1,4]diazepin-2-one was dissolved in 10 ml of dimethoxyethane, to which 0.11 g of sodium hydrogencarbonate and 0.22 g of phosphorus pentasulfide were added, followed by heating at 80° C. for 3 hours. After completion of the reaction, dichloromethane and methanol were added, and the mixture was filtered, followed by addition of silica gel to the resultant filtrate and evaporating the solvent to dryness. Silica gel column chromatography (elution solvent: dichloromethane:methanol=99:1) was used for purification, thereby obtaining 0.15 g of the intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409909
Source datasetuspto-grants-1995_04
ORD IDord-2623954b0bb44318b9a051422a448447
Source noteuspto-grants-1995_04