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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254792Generated: October 25, 2026

Hydrochloric Acid → (S)-2-Amino-3-(4-(4-(4-phenoxyphenyl)-1H-1,2,3-triazol-1-yl)phenyl)propanoic acid

https://huagongshe.com/reaction/254792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoc-4-azido-L-phenylalanineHCID 11243693—
Reactant1-Ethynyl-4-phenoxybenzeneHCID 12788024—
SolventMethanolHCID 887—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
Product(S)-2-Amino-3-(4-(4-(4-phenoxyphenyl)-1H-1,2,3-triazol-1-yl)phenyl)propanoic acidHCID 2363339229%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-ethynyl-4-phenoxy-benzene (126 mg, 0.65 mmol) and (S)-3-(4-azido-phenyl)-2-tert-butoxycarbonylamino-propionic acid (200 mg, 0.65 mg) in H2O:dioxane (5:1) was heated at 100° C. in a sealed tube for overnight. After completion of reaction, 3N HCl (5 ml) was added and the mixture was stirred for 2 hr at 50° C. Removal of solvent gave crude product which was dissolved in MeOH and purified by preparative HPLC to give 45 mg of desired product (yield: 29%). 1H-NMR (400 MHz, CD3OD): δ (ppm) 3.2 (m, 1H), 3.4 (m, 1H), 4.3 (m, 1H), 6.9 (d, 2H), 7.0 (d, 2H), 7.2 (m, 1H), 7.3 (d, 2H), 7.4-7.55 (m, 6H), 8.0 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875622B2
Source datasetuspto-grants-2011_01
ORD IDord-09486fd8d5fa449f9b808cacf9a40af3
Source noteuspto-grants-2011_01