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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027639Generated: October 27, 2026

Triethylamine → Methyl 5-(2-(benzyloxycarbonylamino)-4-methylpentanamido)-2-hydroxybenzoate

https://huagongshe.com/reaction/1027639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 5-amino-2-hydroxybenzoateHCID 135127—
Reactant2-(((Benzyloxy)carbonyl)amino)-4-methylpentanoic acidHCID 246673—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventAcetonitrileHCID 6342—
ProductMethyl 5-(2-(benzyloxycarbonylamino)-4-methylpentanamido)-2-hydroxybenzoateHCID 5919317151.8%

Reaction Steps

A mixture of 2-(benzyloxycarbonylamino)-4-methylpentanoic acid (1 g, 3.8 mmol), methyl 5-amino-2-hydroxybenzoate (0.66 g, 3.95 mmol) and Et3N (0.76 g, 7.6 mmol) were dissolved in CH3CN (10 mL) and HATU (1.503 g, 3.95 mmol) was added. The mixture was stirred (RT, 16 h). The solvent was removed under reduced pressure. Brine (50 mL) was added to the resulting residue, and the mixture was extracted with EtOAc (3×50 mL). The combined organic layers were washed successively with 2N aq. HCl (3×50 mL), brine (50 mL), 5% NaHCO3 (50 mL×3), brine (50 mL), dried over MgSO4, filtered, and concentrated under reduced pressure. The crude material was purified by silica chromatography on (CH2Cl2) to give methyl 5-(2-(benzyloxycarbonylamino)-4-methylpentanamido)-2-hydroxybenzoate as a white solid (0.81 g, 51.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735379B2
Source datasetuspto-grants-2014_05
ORD IDord-acd92a29eb6644c5adea00f69799e566
Source noteuspto-grants-2014_05