HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64531Generated: October 26, 2026
N,N-Dimethyl-1,3-propanediamine → gamma-benzyl-L-glutamic acid Nepsilon-benzyloxycarbonyl-L-lysine
https://huagongshe.com/reaction/64531
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | HCID 54303727 | HCID 54303727 | — |
| Reactant | N-carboxy-N'-benzyloxycarbonyl-L-lysine anhydride | HCID 86718959 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | gamma-benzyl-L-glutamic acid Nepsilon-benzyloxycarbonyl-L-lysine | HCID 86718960 | — |
Reaction Steps
To 1,2-dichloroethane (10 ml) was added N-carboxy-γ-benzyl-L-glutamic acid anhydride (1.00 g, 3.80 mmol), and the mixture was cooled to 0° C. N,N-Dimethyl-1,3-propanediamine (0.48 μl, 3.8 μmol) was added as an initiator, and the mixture was stirred at 25° C. for 1 day and cooled again to 0° C. Nα-Carboxy-Nε-benzyloxycarbonyl-L-lysine anhydride (1.16 g, 3.80 mmol) was added, and the mixture was stirred at 25° C. for 3 days to give a γ-benzyl-L-glutamic acid-Nε-benzyloxycarbonyl-L-lysine block copolymer (high molecular weight copolymer). The weight average molecular weight, Mw, of the copolymer was measured by Measurement Method 1 described below. In addition, the composition of the copolymer was measured by Measurement Method 2 described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09450174B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-75f47b78ea394291bac57610d5878932 |
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| Source note | uspto-grants-2016_09 |
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