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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981330Generated: October 30, 2026

Dichloromethane → HCID 178478812, compound

https://huagongshe.com/reaction/981330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178467837HCID 178467837—
ProductHCID 178478812HCID 17847881212.9%

Reaction Steps

1.32 g (1.70 mmol) of 19-[2,3-bis(t-butoxycarbonyl)guanidino]-11-t-butyldimethylsilyloxy-1,1-diethoxy-4,9,12-triazanonadecane-10,13-dione was dissolved in 1 ml of methylene chloride and 5 ml of trifluoroacetic acid was added dropwise thereto under ice-cooling. After reacting at room temperature for 2.5 hours, the solvent was distilled off under reduced pressure. The residue was dissolved in 100 ml of distilled water and the pH value of the obtained solution was adjusted to 4.5 with 1N NaOH. The aqueous solution thus obtained was adsorbed on 120 ml of CM-Sephadex® C-25 (Na) and subjected to gradient elution between 500 ml of distilled water and 500 ml of 0.5M NaCl. Fractions containing the aimed compound were combined, adsorbed on 20 ml of granular Shirasagitan® KLH-250 and subjected to gradient elution between 500 ml of distilled water and a 50% aqueous solution of acetonitrile. Fractions positive to Sakaguchi's reagent were combined and concentrated under reduced pressure to thereby reduce the volume to one-tenth of the original. Some portion of the concentrate was collected and determined. Thus it was found that the concentrate contained 101 mg of the aimed compound (yield: 12.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990536
Source datasetuspto-grants-1991_02
ORD IDord-d0c8ed8d78cf401984464daf577e2d5f
Source noteuspto-grants-1991_02