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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339926Generated: October 30, 2026

Water → Methyl-(s)-1-[(s)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl-amino]-1-oxo-3-phenylpropan-2-ylcarbamate

https://huagongshe.com/reaction/339926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl chloroformateHCID 6586—
ReactantTert-butyl (5)-1-[(5)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethylamino]-1-oxo-3-phenylpropan-2-ylcarbamateHCID 57943172—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl-(s)-1-[(s)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl-amino]-1-oxo-3-phenylpropan-2-ylcarbamateHCID 57943180—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-butyl (S)-1-[(S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethylamino]-1-oxo-3-phenylpropan-2-ylcarbamate, 8, (0.460 mg, 0.881 mmol) is dissolved in a solution of 4M hydrogen chloride in 1,4-dioxane (4 mL). The reaction mixture is stirred 1 hour, and the solvent is removed under reduced pressure. The resulting crude amine is dissolved in CHCl3 (8 mL) and pyridine (1 mL) is added. The temperature is cooled to 0° C. and methyl chloroformate (0.083 g, 0.881 mmol) is added dropwise. The reaction mixture is allowed to warm to room temperature and stirred for 2 days. Water is added, the solution stirred for 15 minutes and then extracted several times with CHCl3. The combined organic layers are washed with 1N HCl, 5% NaHCO3, and brine, dried over Na2SO4, and filtered. The solvent is removed in vacuo to afford 0.297 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895563B2
Source datasetuspto-grants-2014_11
ORD IDord-2c51f178f3364eea8c607690840233c5
Source noteuspto-grants-2014_11