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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383466Generated: October 31, 2026

HCID 44466646, compound → HCID 44466646, compound

https://huagongshe.com/reaction/383466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 44466646HCID 44466646—
Reactanthydroxylamine NaHCO3HCID 86656236—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 44466646HCID 44466646—
ProductHCID 76770971HCID 76770971—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-(2-(3,5-Dimethylisoxazol-4-yl)-3-thiocyanato-1H-indol-1-yl)phenol was dissolved in DMSO and 10 eq 2 M hydroxylamine/NaHCO3 (aq) stock solution was added. The reaction was stirred at 65° C. overnight and then diluted with H2O. A precipitation was formed after stirring for 5 min. The mixture was diluted with EtOAc and diethylether, washed with NH4Cl (aq) and phases were partitioned. Organic phase was evaporated to dryness in vacuo and subjected to purification on reverse phase preparative HPLC to provide the title compound 2-(3,5-dimethylisoxazol-4-yl)-1-(4-hydroxyphenyl)-1H-indol-3-yl N′-hydroxycarbamimidothioate (E32). ES/MS m/z: 395.17 (M+H), 393.19 (M−H); 1H NMR (acetone-d6, 500 MHz): 8.88 (broad s, 1H), 8.73 (broad s, 1H), 7.80-7.78 (m, 1H), 7.29-7.24 (m, 3H), 7.18 (d, 2H), 6.95 (d, 2H), 5.11 (broad s, 2H), 2.28 (s, 3H), 2.00 (s, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367665B2
Source datasetuspto-grants-2013_02
ORD IDord-2ed156d344b4416db290aaa9dca09ad6
Source noteuspto-grants-2013_02