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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459145Generated: November 1, 2026

Hydrogen Bromide → HCID 88323774, compound

https://huagongshe.com/reaction/1459145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHCID 131720995HCID 131720995—
ReactantHCID 131720997HCID 131720997—
SolventAcetic AcidHCID 176—
ProductHCID 88323774HCID 88323774—

Reaction Steps

N-(N-(N-(N-(N-Sarcosyl-N-(4-oxo-4-(4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)phenylamino)butanoyl)lysyl)glycyl)phenylalanyl)leucyl)glycine N-(2-sarcosyl-aminoethyl)amide dihydrobromide. It is contemplated that N-(N-(N-(N-(N-(N-(Phenylmethoxycarbonyl)sarcosyl)-N-(4-oxo-4-(4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)phenylamino)butanoyl)lysyl)glycyl)phenylalanyl)leucyl)glycine N-(2-(N-(phenylmethoxycarbonyl)sarcosylamino)ethyl)amide is stirred with 30% hydrogen bromide in acetic acid for 1 h. The solvent and excess reagent is evaporated under reduced pressure. Trituration of the residue with five portions of dry diethyl ether give N-(N-(N-(N-(N-sarcosyl-N-(4-oxo-4-(4-(10,15,20-triphenyl-21H,23H-porphin-5-yl)-phenylamino)butanoyl)lysyl)glycyl)phenylalanyl)leucyl)glycine N-(2-sarcosylamino-ethyl)amide dihydrobromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853713
Source datasetuspto-grants-1998_12
ORD IDord-5bdb1d8f37814cf2a750db060cd4fcb1
Source noteuspto-grants-1998_12