HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722985Generated: October 29, 2026
Hydrochloric Acid → HCID 131726071, compound
https://huagongshe.com/reaction/722985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- | HCID 85083 | — |
| Reactant | HCID 131726072 | HCID 131726072 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | HCID 131726071 | HCID 131726071 | 98% |
Reaction Steps
At 0° C. the solution of 657 mg (1.28 mmol) of HCl.Ala-Lys(ClZ)-OBzl in 5 ml of anhydrous tetrahydrofuran was adjusted to pH 9, to which the pre-cold solution of 280 mg (1.3 mmol) of Boc-Pro-OH, 170 mg (1.26 mmol) of 1-hydroxybenzotriazole and 270 mg (1.31 mmol) of dicyclohexylcarbodiimide in 30 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, 20:1) indicated complete disappearance of HCl.Ala-Lys(ClZ)-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 134 mg (98%) of the title compound as a colorless powder. Mp86–88° C., FAB-MS (m/e) 674[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07138491B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-2421226033764d76b6c7837cbee02081 |
|---|
| Source note | uspto-grants-2006_11 |
|---|