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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446186Generated: October 29, 2026

1-Hydroxybenzotriazole → 2-{(1R,3R)-1-[(2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoyloxy]-4-methyl-3-methylamino-pentyl}-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/446186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactanttert-Butoxycarbonyl-L-isoleucineHCID 2724762—
ReactantEthyl 2-((1R,3R)-1-hydroxy-4-methyl-3-(methylamino)pentyl)thiazole-4-carboxylateHCID 24906126—
SolventDichloromethaneHCID 6344—
Product2-{(1R,3R)-1-[(2S,3S)-2-tert-Butoxycarbonylamino-3-methyl-pentanoyloxy]-4-methyl-3-methylamino-pentyl}-thiazole-4-carboxylic acid ethyl esterHCID 24906127—

Reaction Steps

A 0.1 M solution of N-methyl tubuvaline ethyl ester 35 (0.305 g, 1.06 mmol), 1-hydroxybenzotriazole (HOBt) (0.146 g, 1.08 mmol), and Boc-Ile-OH (0.267 g, 1.11 mmol) in CH2Cl2 (10.6 mL) was cooled in a salted ice-water bath. PS-CCD (1.38 mmol/g, 0.920 g, 1.27 mmol) was added with stirring, and the bath was warmed to rt. Stirring was continued for 14 h, the solution was filtered, and the resin was washed with CH2Cl2. The filtrate was then concentrated, diluted with EtOAc, and washed once with sat. NaHCO3 (aq). The aqueous fraction was back-extracted twice with EtOAc, and the combined organic fractions were dried with Na2SO4, filtered, and concentrated to afford intermediate 36, which was taken on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476451B2
Source datasetuspto-grants-2013_07
ORD IDord-a17e76c38193417a80a97c58ec57a7fe
Source noteuspto-grants-2013_07