HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723013Generated: October 30, 2026
Hydrochloric Acid → HCID 178427547, compound
https://huagongshe.com/reaction/723013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | HCID 178427561 | HCID 178427561 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 178427547 | HCID 178427547 | 54% |
Reaction Steps
At 0° C. the solution of 45 mg (0.072 mmol) of HCl.Arg(Tos)-Pro-Ala-OBzl in 15 ml of anhydrous tetrahydrofuran was adjusted to pH 9, to which the pre-cold solution of 15 mg (0.079 mmol) Boc-Ala-OH, 10 mg (0.074 mmol) of 1-hydroxybenzotriazole and 16 mg (0.077 mmol) of dicyclohexylcarbodiimide in 20 ml of anhydrous tetrahydrofuran was added. The reaction mixture was stirred at 0° C. for 2 h and at room temperature for 6 h and TLC (chloroform/methanol, 30:1) indicated complete disappearance of HCl.Arg(Tos)-Pro-Ala-OBzl. The resulted precipitates of N,N-dicyclohexylurea were filtrated and the filtrate was diluted with 80 ml of ethyl acetate. The solution obtained was washed successively with saturated NaCO3 in water (50 ml×3), saturated NaCl in water (50 ml×3) and KHSO4 in water (5%, 30 ml×3). The separated ethyl acetate layer was dried with anhydrous MgSO4, and then evaporated to provide 30 mg (54%) of the title compound as a colorless powder. Mp 80–82° C., FAB-MS (m/e) 758[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138491B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-55fbe66b0abb48f9905135f48eb04836 |
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| Source note | uspto-grants-2006_11 |
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