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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976423Generated: November 1, 2026

Hydrochloric Acid → HCID 57110839, compound

https://huagongshe.com/reaction/1976423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant1,4-Dioxane--water (1/1)HCID 21886435—
ReactantHCID 57144254HCID 57144254—
ReactantHCID 86587116HCID 86587116—
ProductHCID 57110839HCID 5711083983%

Reaction Steps

The (2S)-2-amino-3-[(3-hydroxypropyl)sulfanyl]-3-methylbutanoic acid was dissolved in dioxane:water (1:1) (40 mL). Triethylamine (5.1 mL, 50.4 mmol) was added to the solution followed by 2-butynyloxybenzenesulfonyl chloride (4.1 g, 16.8 mmol). The resulting mixture was stirred for 15 h at room temperature. The mixture was acidified to pH ˜2 with 1N hydrochloric acid and partitioned between ethyl acetate and water. The organic layer was dried over anhydrous sodium sulfate. Removal of the solvent gave 5.78 g (83%) of (2S)-2-({[4-(2-butynyloxy)phenyl]sulfonyl}amino)-3-[(3-hydroxypropyl)sulfanyl]-3-methylbutanoic acid as a solid; 1H NMR (300 MHz, acetone-d6) δ 1.34 (s, 3H), 1.39 (s, 3H), 1.66 (m, 2H), 2.06 (m, 3H), 2.54-2.68 (m, 2H), 3.89 (m, 1H), 4.82 (m, 2H), 6.56 (d, 1H, J=9.0 Hz), 7.12(d, 2H, J=8.7 Hz), 7.81(d, 2H, J=8.7 Hz). HRMS (C18H25NOS2)(M+H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225311B1
Source datasetuspto-grants-2001_05
ORD IDord-c79b670f9fb94589b41e2b37c2de3da8
Source noteuspto-grants-2001_05