HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459074Generated: October 29, 2026
Hydrochloric Acid → HCID 131726301, compound
https://huagongshe.com/reaction/459074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Alanine 1,1-dimethylethyl ester | HCID 89016 | — |
| Reactant | Boc-glu(obzl)-osu | HCID 13242221 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131726301 | HCID 131726301 | — |
Reaction Steps
Boc-L-Glu(OBzl)OSu (Bachem), 434 mg (1 mmol) is reacted with L-Ala-OtBu. HCl, 182 mg (1 mmol) in 10 mL DMF containing triethylamine (202 mg). After stirring for 16 hours at room temperature, the reaction mixture is rotary evaporated to dryness and the residue is redissolved in methylene chloride, washed with water, dried over sodium sulfate and evaporated to dryness. The residue is redissolved in methanol, 50 mL, and transferred to a Parr flask. 10% Pd/C catalyst (Aldrich), 50 mg, is added and the flask is charged with 40 psi hydrogen gas on a Parr shaker. The mixture is shaken for 2 hours at room temperature or until no further consumption of hydrogen is noted. The Parr flask is evacuated and charged with argon gas. The mixture is filtered through Celite, and the filtrate is rotary evaporated to give crude Boc-L-Glu-L-Ala-OtBu.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07193065B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-ccb3ebcfa7054f07af03fb2b536f9258 |
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| Source note | uspto-grants-2007_03 |
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