Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycine | HCID 750 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Z-Glp-Pro-OH | HCID 13817306 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Z-Glp-Pro-Gly-OH | HCID 131732954 | — |
Reaction Steps
Two solutions were prepared before the peptide coupling. Solution A: H-Gly-OH (1.2 eq.) was dissolved in MSA (3.0 eq.) at maximum 60° C. The suspension was cooled down to 25° C., diluted with DCM and stirred for at least 8 hours before being cooled to −15° C. In solution B, the carboxylic function of the Z-Glp-Pro-OH was dissolved with DCM and NMM (1.05 eq.). The solution was cooled to −15° C. The carboxylic acid was activated with IBCF (1.05 eq.) and the silylated solution A was then added to the slurry. The slurry was stirred for at least 0.5 h and left to warm to 25° C. The mixture was quenched with water and the addition of a solution of KHSO4 under stirring precipitated the peptide. The solid was filtered and washed with water. After drying under vacuum, 80% of Z-Glp-Pro-Gly-OH was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051349B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-29a656e543784974becb02ef80e04fbc |
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| Source note | uspto-grants-2015_06 |
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