HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoindane → 3(S)-(2-((2(S)-(Benzoyl)amino-3-methylbutyryl)-(1,3-dihydroisoindol-2-yl)amino)acetylamino)-4-oxo-butyric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Reactant | 1,3-Dihydro-2H-isoindol-2-amine | HCID 12735618 | — |
| Reactant | 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-oxo-butyric Acid | HCID 54405243 | — |
| Product | 3(S)-(2-((2(S)-(Benzoyl)amino-3-methylbutyryl)-(1,3-dihydroisoindol-2-yl)amino)acetylamino)-4-oxo-butyric Acid | HCID 54120604 | — |
Reaction Steps
Compound 756 was prepared by a method similar to the method used to prepare compound 724 and compound 706, except 2-aminoindane was replaced with 2-aminoisoindoline (prepared as described in Eloy, F., Moussebois, C., Bull. Soc. Chim. Belg., 68, pp. 409-421 (1959)). ##STR136##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05843904 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-bf7c302022864f00923a0985f670be93 |
| Source note | uspto-grants-1998_12 |