HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 5-((4-(5-(4-propylphenyl)-1,2,4-oxadiazol-3-yl)indolin-1-yl)methyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate → HCID 46195603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 5-((4-(5-(4-propylphenyl)-1,2,4-oxadiazol-3-yl)indolin-1-yl)methyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 86661797 | — |
| Reactant | HCID 86661798 | HCID 86661798 | — |
| Product | HCID 46195603 | HCID 46195603 | 80% |
Reaction Steps
When the product of Step C was substituted for tea-butyl 5-((4-(5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl)indolin-1-yl)methyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate in Example 34, Step E, the identical process afforded the title compound in 80% yield, as a creamy solid. 1H-NMR (DMSO-d6) 0.85-0.95 (m, 3H); 1.33 (broad s, 2H); 2.6-2.66 (m, 2H); 2.98 (s, 2H); 3.2-3.34 (m, 8H+H2O); 3.54 (tr, 2H, J=8.3 Hz); 4.56 (broad s, 2H); 6.77 (d, 1H, J=7.77 Hz); 7.1-7.26 (m, 2H); 7.38-7.49 (m, 2H); 7.9-8.1 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181182B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-32cc86c197bd45398b67585d44acb396 |
| Source note | uspto-grants-2015_11 |