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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062093Generated: October 26, 2026

4-Chloro-1-hydroxy-2-naphthoic acid → 2-[(4-Chloro-1-hydroxy-naphthalene-2-carbonyl)-amino]-2-methyl-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2062093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1-hydroxy-2-naphthoic acidHCID 79416—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantTert-butyl 2-amino-2-methylpropanoate hydrochlorideHCID 12186776—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[(4-Chloro-1-hydroxy-naphthalene-2-carbonyl)-amino]-2-methyl-propionic acid tert-butyl esterHCID 6670116628%

Reaction Conditions

Temperature60 °C

Reaction Steps

2.25 g of 4-chloro-1-hydroxy-naphthalene-2-carboxylic acid, 3.57 2-amino-2-methyl-propionic acid tert-butyl ester hydrochloride, 6.93 g HATU and 5.29 mL of N,N′diisopropylethylamine were dissolved in 100 mL of dimethylformamide. The reaction was heated at 60° C. for 1.5 hour followed by room temperature overnight. Water was added and the mixture was extracted with diethyl ether twice. The combined organic layers were dried with magnesium sulfate and concentrated in vacuo. Purification by flash chromatography on silica with heptanes/ethyl acetate afforded 1.016 g (28%) of 2-[(4-chloro-1-hydroxy-naphthalene-2-carbonyl)-amino]-2-methyl-propionic acid tert-butyl ester as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283479B2
Source datasetuspto-grants-2012_10
ORD IDord-3f5a1be694b4499f856d18eb57c0fec9
Source noteuspto-grants-2012_10