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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018868Generated: November 1, 2026

2-Aminothiazole → HCID 10135824, compound

https://huagongshe.com/reaction/1018868

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(S)-3-cyclohexyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamideHCID 9947513—
ReactantHCID 69694579HCID 69694579—
ProductHCID 10135824HCID 1013582432.7%

Reaction Steps

BOP coupling of (S)-3-cyclohexyl-2-(4-Chloro-1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid (ca. 1:1 mixture of regioisomers, prepared in Step C; 326 mg; 1.0 mmol) and 2-aminothiazole (231 mg; 2.23 mmol) in a manner similar to that used for the preparation of (S)-3-cyclohexyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide as outlined in Example 9, Step B) provided after chromatography (Biotage 40M column, eluent: 5% to 30% gradient of ethyl acetate/hexanes) 132 mg of (S)-3-Cyclohexyl-2-(4-Chloro-1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide: EI-HRMS m/e calcd for C20H22ClN3O2S (M++Na+) 426.1013, found 426.1016; and 91 mg of regioisomeric (S)-3-Cyclohexyl-2-(7-Chloro-1-oxo-1,3dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide: EI-HRMS m/e calcd for C20H22ClN3O2SNa (M++Na+) 426.1013, found 426.1017.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482951B2
Source datasetuspto-grants-2002_11
ORD IDord-ee4703a50fe34bdca0679e0a604a4dd5
Source noteuspto-grants-2002_11