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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916819Generated: November 1, 2026

HCID 69391369, compound → HCID 69387222, compound

https://huagongshe.com/reaction/916819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69391369HCID 69391369—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 69387222HCID 69387222—
ProductHCID 69405869HCID 69405869—

Reaction Steps

N-(tert-Butoxycarbonyl)-N-[3-({2-[4-(2-{[(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]amino}ethyl)phenoxy]ethoxy}methyl)phenyl]sulfamide (15 mg) in acetic acid (1.5 ml) and water (0.5 ml) was heated at 75° C. for 0.5 h. The solution was then concentrated in vacuo and azeotroped with MeOH. The residue was purified by HPLC to give the title compounds N-{3-[(2-{4-[2-({(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)ethyl]phenoxy}ethoxy)methyl]phenyl}sulfamide formate (1.5 mg) LCMS RT=2.21 min, ES+ve 532 (MH)+and N-(tert-butoxycarbonyl)-N-{3-[(2-{4-[2-({(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino)ethyl]phenoxy}ethoxy)methyl]phenyl}sulfamide formate (0.9 mg). LCMS RT=2.51 min ES+ve 630 (MH)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271197B2
Source datasetuspto-grants-2007_09
ORD IDord-1a5876815d854db096666edb379bd9c3
Source noteuspto-grants-2007_09