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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784243Generated: October 30, 2026

1-Naphthaldehyde → (S)-3-(4-Bromo-phenyl)-2-{4-[(naphthalen-1-ylmethyl)-amino]-benzoylamino}-propionic acid methyl ester

https://huagongshe.com/reaction/1784243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantDichloromethaneHCID 6344—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(S)-2-(4-Amino-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl esterHCID 68861436—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-(4-Bromo-phenyl)-2-{4-[(naphthalen-1-ylmethyl)-amino]-benzoylamino}-propionic acid methyl esterHCID 6886001148%

Reaction Steps

(S)-3-(4-Bromo-phenyl)-2-{4-[(naphthalen-1-ylmethyl)-amino]-benzoylamino}-propionic acid methyl ester (273 mg) was prepared from (S)-2-(4-amino-benzoylamino)-3-(4-bromo-phenyl)-propionic acid methyl ester (415 mg, 1.1 mmol) and 1-naphthaldehyde (0.331 mL, 2.4 mmol) according to Procedure G, except for the following: the reaction was done in 15 mL DCE and 5 mL THF, was allowed to stir for 15 min before NaBH(OAc)3was added, was treated with two additional equiv. NaBH(OAc)3 after 2 h, and an adapted work-up. After reaction completion, 100 mL of DCM was added and the organic washed with saturated sodium bicarbonate, dried over sodium sulfate, and evaporated. The crude material was triturated with MeOH.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501538B2
Source datasetuspto-grants-2009_03
ORD IDord-e2ac4afce6ba4e8f952e9cac82745271
Source noteuspto-grants-2009_03