Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Z-Nle-OH | HCID 6993403 | — |
| Reactant | HCID 25797686 | HCID 25797686 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 131712420 | HCID 131712420 | — |
Reaction Steps
4.95 g of Z-Nle-OH dissolved in 50 ml tetrahydrofuran are cooled to -20° C. and 2.1 ml of N-methylmorpholine followed by 2.43 ml of chloroformic acid isobutylester are added to the solution with stirring. The solution is stirred for a further 10 minutes at -15° C. and a cold solution comprising 10.6 g of H-Asn-Phe-Phe-OMe. hydrobromide and 2.5 ml of N-methylmorpholine in 60 ml N,N-dimethylformamide/tetrahydrofuran (1:1) are added. The solution is stirred for 20 hours at 0° C. and for 2 hours at room temperature and subsequently stirred with aqueous ethanol. After filtration, washing with (a) methanol and (b) ether and drying, the title compound is obtained [α]D20 =-31° (c=1.0 in dimethylformamide): decomposition at 235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04291022 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-b9170776db75435b8a04a385a26ffea8 |
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| Source note | uspto-grants-1981_09 |
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