HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415338Generated: November 1, 2026
Hydrochloric Acid → HCID 178465163, compound
https://huagongshe.com/reaction/1415338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 73909582 | HCID 73909582 | — |
| Reactant | HCID 178465166 | HCID 178465166 | — |
| Reactant | HCID 178476397 | HCID 178476397 | — |
| Catalyst | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178465163 | HCID 178465163 | 86.8% |
Reaction Steps
In analogy to Example 8(b) 3.6 g (6.8 mmols) of H-Cys(But)-Arg-Pro-NH-C2H5 . 2 HCl were reacted with 3 g of Z-D-Leu-OTcp and worked up. The oily residue (6.1 g of contaminated Z-D-Leu-Cys(But)-Arg-Pro-NH--C2H5) was hydrogenated catalytically in analogy to Example 8(b). Yield: 2.5 g (57%). The compound was strongly contaminated and purified over Sephadex LH 20 in analogy to Example 1(a). Yield: 1.734 g (40%) of H-D-Leu-Cys(But)-Arg-Pro-NH-C2H5 -diacetate. The 1.734 g (2.7 mmols) of H-D-Leu-Cys(But)-Arg-Pro-NH-C2H5 -acetate were reacted in analogy to Example 8(b) with 1.33 g of Z-Ser-Tyr(Bzl)-OH, 0.71 ml of N-ethyl morpholine, 3.65 mg of HOBt and 595 mg of DCC in 5 ml of dimethylformamide and worked up. The substance obtained (2.45 g of Z-Ser-Tyr(Bzl)-D-Leu-Cys(But)-Arg-Pro-NH-C2H5) was hydrogenated catalytically in analogy to Example 8(b) and purified over Sephadex LH 20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04003884 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-cc6834bc20944f83983d5518656fa2ee |
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| Source note | uspto-grants-1977_01 |
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