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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234241Generated: October 31, 2026

Hydrochloric Acid → HCID 178493316, compound

https://huagongshe.com/reaction/234241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantTrisodium PhosphateHCID 24243—
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
ReactantHCID 53857414HCID 53857414—
ProductHCID 178493316HCID 17849331624%

Reaction Steps

The pH of a suspension of 20 mg of the product of Example 130 in 3 ml of 0.05M pH7 sodium phosphate buffer was adjusted to 8.5 by the addition of 0.1N sodium hydroxide. Over 3 h, 74 mg of ethyl acetimidate hydrochloride were added in small portions, the pH of the reaction mixture being maintained at 8.5. The mixture was set to pH 7 by addition of 1N hydrochloric acid and then extracted with ethyl acetate. The aqueous phase was concentrated in vacuo and chromatographed on MCI-Gel CHP20P (Mitsubishi Chemical Industries, Ltd.) using at first 1% aqueous acetic acid and then mixtures of 1% aqueous acetic acid with acetonitrile (10:1 to 2:1, v/v). The product-containing fractions were lyophilized to yield 4 mg of (4R)-N-[5-(16-hydroxy-14-methoxy-13-methyl-12-oxo-6-thioxo-1,3,4,5,6,7,8,9,10,12-decahydro-11,2,5-benzoxathiaazacyclotetradecin-4-yl)-1,2,4-oxadiazol-3-ylmethyl]-acetimidamide hydroacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594135
Source datasetuspto-grants-1997_01
ORD IDord-eb6220133454480eb820cb4d5d3608d6
Source noteuspto-grants-1997_01