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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018849Generated: October 29, 2026

2-Aminothiazole → 3-Cycloheptyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide

https://huagongshe.com/reaction/1018849

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—
Reactant3-Cycloheptyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acidHCID 18402168—
Product3-Cycloheptyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamideHCID 1027131697.6%

Reaction Steps

BOP coupling of 3-Cycloheptyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionic acid (prepared in Step E; 173 mg; 0.58 mmol) and 2-aminothiazole (97 mg; 0.94 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 1, Step B) provided after flash chromatography (Biotage 40S, eluent: 35% ethyl acetate/hexanes) 217 mg (99%) of 3-Cycloheptyl-2-(1-oxo-1,3-dihydro-isoindol-2-yl)-N-thiazol-2-yl-propionamide as a white foam EI-HRMS m/e calcd for C21H25N3O2S (M+) 383.1667, found 383.1660.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482951B2
Source datasetuspto-grants-2002_11
ORD IDord-fa289b5f15f14ddbab5ef53faf5ed938
Source noteuspto-grants-2002_11