HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 5-((4-(3-(4-fluorophenylamino)prop-1-ynyl)phenyl)-ethynyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate → tert-Butyl-5-(4-(3-(4-fluorophenylamino)propyl)phenethyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 5-((4-(3-(4-fluorophenylamino)prop-1-ynyl)phenyl)-ethynyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 91584153 | — |
| Reactant | tert-Butyl-5-((4-(N-(6,6-dimethylbicyclo[3.1.1]heptan-2-yl)sulfam-oyl)phenyl)ethynyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 131733945 | — |
| Product | tert-Butyl-5-(4-(3-(4-fluorophenylamino)propyl)phenethyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate | HCID 131733946 | 94% |
Reaction Steps
When the product of Step B was substituted for tert-butyl-5-((4-(N-(6,6-dimethylbicyclo[3.1.1]heptan-2-yl)sulfamoyl)phenyl-)ethynyl)-2,2-dimethyl-1,3-dioxan-5-ylcarbamate in Example 19, Step C, the similar process afforded the title compound in 94% yield, as creamy gum. 1H-NMR (CDCl3) 1.42 (s, 3H); 1.44 (s, 3H); 1.46 (s, 9H); 1.87-1.96 (m, 4H); 2.5-2.56 (m, 2H); 2.67 (tr, 2H, J=7.32 Hz); 3.04 (tr, 2H, J=7.05 Hz); 3.86 (d, 2H, J=11.8 Hz); 3.88 (d, 2H, J=11.7 Hz); 4.9 (s, 1H); 6.45-6.50 (m, 2H); 6.82-6.88 (m, 2H); 7.09 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181182B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-20ac875a84ab412e8ea9f9d908c56dd9 |
| Source note | uspto-grants-2015_11 |