HuagongsheHuagongshe Chemistry Print Report · For research reference only
3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-oxobutyric Acid → 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)indan-2-ylamino)acetylamino)-4-(4-(3,5-dichlorophenyl)oxazol-2-yl)-4-oxobutyric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-oxobutyric Acid | HCID 53686139 | — |
| Reactant | ((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetic Acid | HCID 53859725 | — |
| Reactant | 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)benzylamino)acetylamino)-4-(4-(2,6-dichlorophenyl)-oxazol-2-yl)-4-hydroxybutyric Acid tert-Butyl Ester | HCID 54440848 | — |
| Product | 3(S)-(2-((2(S)-Benzoylamino-3-methylbutyryl)indan-2-ylamino)acetylamino)-4-(4-(3,5-dichlorophenyl)oxazol-2-yl)-4-oxobutyric Acid | HCID 53632600 | — |
Reaction Steps
Compound 727 was prepared by a method similar to the method use to prepare compound 710, except compound 704 is replaced with compound 724 in the preparation of compound 708: 1H NMR (500 MHz, CD3OD) δ 8.73 (d), 8.38-8.21 (m), 8.20-8.11 (m), 7.81-7.72 (m), 7.50-7.32 (m), 7.14-6.93 (m), 5.52-5.40 (m), 5.22-5.13 (m), 5.08 (m), 4.96 (d), 4.56 (d), 4.48-4.37 (m), 4.21-4.10 (m), 3.98 (t), 3.82 (d), 3.26-3.11 (m), 3.10-2.88 (m), 2.25-2.12 (m), 1.04-0.83 (m). ##STR106##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05843904 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-5b3f9cbf8e7c4889a1fcce2b7abef487 |
| Source note | uspto-grants-1998_12 |