HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341746Generated: October 31, 2026
Dichloromethane → HCID 131721057, compound
https://huagongshe.com/reaction/341746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | L-Leucine, N-((1,1-dimethylethoxy)carbonyl)- | HCID 83170 | — |
| Product | HCID 131721057 | HCID 131721057 | — |
Reaction Steps
Separately, 2 mmol amino-group-protected amino acid Boc-Leu--OH corresponding to the amino acid residue at the 27-position in SEQ ID NO:1 was dissolved in 4 ml DCM. This solution was introduced into a vessel for amino acid activation, and after 3 ml DCC (0.5M in DCM) and 4 ml HOBt (0.5M in DCM) were added to it, and they were reacted for 30 minutes. Thereafter, the reaction solution was filtered off and the filtrate was transferred to a concentration vessel. 3 ml DMF was added to it and the DCM was distilled off in an argon stream. Then, 3 ml DMF was added to the concentrate, and it was transferred to the above reactor for peptide solid-phase synthesis and reacted for 30 minutes. Then, the reaction mixture was washed with 8 ml DCM (6 times, 20 seconds each). Separately, 2 mmol Boc-Leu--OH was dissolved in 4 ml DCM and the solution was introduced into the reactor for amino acid activation and the same procedure as described above was repeated (double-coupling) and filtered. Boc-Leu-MBHA resin was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856303 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-bebe2ea2acbb48a087d3f3468f48fc0e |
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| Source note | uspto-grants-1999_01 |
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