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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64517Generated: October 27, 2026

Trifluoroacetic acid → 2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid

https://huagongshe.com/reaction/64517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThioanisoleHCID 7520—
ReactantPotassium CarbonateHCID 11430—
ReactantD-Cysteine hydrochloride monohydrateHCID 10176341—
Reactant7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrileHCID 117604981—
SolventDichloromethaneHCID 6344—
Product2-(7-(Leucinyl)aminonaphtho[2,1-d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acidHCID 117604502—

Reaction Steps

7-(Boc-leucinyl)aminonaphtho[2,1-d]thiazole-2-carbonitrile (69 mg, 0.16 mmol) was combined with 0.5 mL of thioanisole and 1.5 mL of DCM and stirred in an ice bath. Trifluoroacetic acid (1.5 mL) was added, and the reaction monitored by HPLC. After 1 h, solvents were removed under reduced pressure, and the remaining residue triturated with ether. The resulting solid was taken up in MeCN/H2O and treated with D-cysteine hydrochloride hydrate (55 mg, 0.31 mmol) and potassium carbonate (55 mg, 0.40 mmol). After 20 min, the reaction was filtered and the product was isolated by preparative HPLC eluting with 2→50% MeCN in 0.1% formic acid. Calcd for C21H23N4O3S2 (M+H): 443.1. found 443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447450B2
Source datasetuspto-grants-2016_09
ORD IDord-3f81971b3c1a40db94d050ff4c49361c
Source noteuspto-grants-2016_09