HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982337Generated: November 2, 2026
Hydrochloric Acid → HCID 178501407, compound
https://huagongshe.com/reaction/1982337
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Benzyloxycarbonyl-beta-alanine | HCID 75313 | — |
| Reactant | Phosphoric acid diphenylester azide | HCID 66782931 | — |
| Reactant | HCID 178501495 | HCID 178501495 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178501407 | HCID 178501407 | — |
Reaction Steps
A solution of 12.3 g of Z-β-Ala-OH and 16.0 g of H-His-OCH3 ×2 HCl in 300 ml of DMF is cooled to 0° and there are added dropwise thereto first a solution of 22.75 g of phosphoric acid diphenyl ester azide in 110 ml of DMF and then a solution of 30.7 ml of triethylamine in 110 ml of DMF. The suspension so obtained is stirred for 2 days at room temperature and then concentrated to an oily suspension in a high vacuum. The residue is taken up in ethyl acetate, washed with sodium bicarbonate and brine, dried and concentrated by evaporation. The crude product is separated by flash chromatography (1.6 kg of silica gel [type 60, Merck], 40-63 μm, 0.4 bar, fractions of 400 ml, eluant: CH2Cl2 /MeOH[13:2]). By concentration by evaporation of the appropriate fractions, Z-β-Ala-His-OCH3 is obtained as a slightly yellowish foam; Rf (L)=0.69.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595677 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-11a883d3500e46388f9181ece59b999f |
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| Source note | uspto-grants-1986_06 |
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