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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184789Generated: October 29, 2026

Hydrochloric Acid → HCID 86758105, compound

https://huagongshe.com/reaction/2184789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydroxylamineHCID 787—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 70103910HCID 70103910—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86758105HCID 86758105—

Reaction Steps

The 1-[(4-methoxyphenyl)sulfonyl]-5-(1-methyl-1H-imidazole4-sulfonyl) diazepine-2-carboxylic acid (0.35 g, 0.76 mmol) is dissolved in methylene chloride (10 mL) at room temperature followed the addition of oxalyl chloride (0.14 mL, 1.56 mmol) and the slow addition of DMF (0.058 mL, 0.76 mmol). This mixture is stirred for 30 minutes at room temperature. In a separate flask, hydroxylamine hydrochloride (0.21 g, 1.56 mmol) in water (2 mL) and THF (5 mL) are stirred at 0° C. and then triethylamine (0.634 mL, 4.56 mmol) is added. This mixture is stirred for 15 minutes. The acid chloride solution is added to the hydroxyl amine solution at 0° C. and the resulting solution is warmed to room temperature and stirred for 3 hours. The solution is acidified to pH˜1 with 1N HCl, poured into water, and extracted with methylene chloride. The organic extracts are dried (Na2SO4) and concentrated down to an oil. The oil is purified by HPLC with a reverse phase column using 80% (95% water, 5% acetonitrile, 0.1% formic acid) and 20% (80% acetonitrile, 20% water) as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399598B1
Source datasetuspto-grants-2002_06
ORD IDord-8dbbcb5e6cab41209db314b608bcee0e
Source noteuspto-grants-2002_06