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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737382Generated: November 1, 2026

(Methoxycarbonylsulfamoyl)triethylammonium hydroxide → HCID 53888673, compound

https://huagongshe.com/reaction/1737382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Methoxycarbonylsulfamoyl)triethylammonium hydroxideHCID 11032497—
ReactantHCID 86753964HCID 86753964—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53888673HCID 5388867346.3%

Reaction Steps

A solution of 10.0 g (0.0279 mol) of methyl (S)-3-hydroxy-2-(5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-ylcarbonylamino)-propionate in 500 ml of tetrahydrofuran was treated while gassing with argon with 7.25 g (0.0304 mol) of methoxycarbonylsulphamoyl-triethylammonium hydroxide internal salt (Burgess reagent) according to the method described in Tetr. Letters 1992, 33, 907. The mixture was boiled at reflux for 1 hr. and completely freed from the solvents. The residue was dissolved in dichloromethane and chromatographed over silica gel with ethyl acetate/ethanol 9:1 as the eluent. There were obtained 4.4 g (46%) of methyl (S)-2-(5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-yl)-4,5-dihydro-oxazole-4-carboxylate as a white solid. An analytical sample was recrystallized from ethanol/diethyl ether and gave white crystals; m.p. 190-192°. [α]D20 =+45.4° (CHCl3, c=1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962450
Source datasetuspto-grants-1999_10
ORD IDord-b0ab65b132774ff8a99ae2351264a6f6
Source noteuspto-grants-1999_10