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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247811Generated: November 2, 2026

Sodium Chloride → tert-butyl {(3S)-4-[(5-amino-1-methyl-1H-pyrazol-4-yl)amino]-3-hydroxy-4-oxobutyl)carbamate

https://huagongshe.com/reaction/1247811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2S)-4-(((tert-butoxy)carbonyl)amino)-2-hydroxybutanoic acidHCID 11816837—
Reactant1H-Pyrazole, 4,5-diamine-1-methyl-, sulfate (1:1)HCID 21904571—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Producttert-butyl {(3S)-4-[(5-amino-1-methyl-1H-pyrazol-4-yl)amino]-3-hydroxy-4-oxobutyl)carbamateHCID 8659340658.9%

Reaction Steps

To a suspension of 1-methyl-1H-pyrazole-4,5-diamine sulfate (86 g) in tetrahydrofuran (1.3 L) was added triethylamine (117 ml), and then (2S)-4-[(tert-butoxycarbonyl)amino]-2-hydroxybutanoic acid (82.5 g) was added to the mixture. To the mixture were added 1-hydroxybenzotriazole (58.3 g) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (82.7 g) under ice-cooling. The reaction mixture was stirred at room temperature for 8 hours. To the reaction mixture were added ethyl acetate (1.3 L), saturated aqueous sodium hydrogen carbonate solution and sodium chloride, and the mixture was stirred for 30 minutes. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (1.0 L) six times. The extract was dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with ethyl acetate/tetrahydrofuran (1/1) to give tert-butyl {(3S)-4-[(5-amino-1-methyl-1H-pyrazol-4-yl)amino]-3-hydroxy-4-oxobutyl}carbamate (69.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129232B2
Source datasetuspto-grants-2006_10
ORD IDord-d173e63b27594994b101f3cde68dcabb
Source noteuspto-grants-2006_10