HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Aminoethyl)-1,3-propanediamine → HCID 17944091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Aminoethyl)-1,3-propanediamine | HCID 26091 | — |
| Reactant | 2-(Benzylamino)acetic acid | HCID 86965 | — |
| Reactant | HCID 53777645 | HCID 53777645 | — |
| Reactant | HCID 54472393 | HCID 54472393 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 17944091 | HCID 17944091 | — |
| Product | HCID 54472393 | HCID 54472393 | — |
Reaction Steps
The p-nitrophenyl ester of N-benzylglycine and N-(2-aminoethyl)-1,3-propane diamine are reacted in the same proportions as in (A) above but in dimethyl formamide as the solvent to yield, after working up in a similar manner, N-(N-benzylglycyl)-N-[2-(benzylaminoacetamido)-ethyl]-3-(benzylaminoacetamido)-propylamine in 65% yield, δ(d6DMSO) 1.6 (m, 2H), 3.2 (m, 6H), 3.5 (d, 4H), 3.8 (d, 2H), 5.0 (s, 6H), 7.3 (s, 15H), 7.4 (m, 3H), 7.8 (m, 3H). Hydrogenation as in (A) above yields the title compound in 75% yield as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666927 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-609af1357b2147b089366d9afda109cd |
| Source note | uspto-grants-1987_05 |