HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-N-Boc-amino-1H-indole → tert-Butyl 4-((4-(5-amino-1H-indol-1-yl)thiazol-2-yl)oxy)-piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-N-Boc-amino-1H-indole | HCID 11458923 | — |
| Reactant | tert-Butyl 4-((4-bromothiazol-2-yl)oxy)piperidine-1-carboxylate | HCID 86696185 | — |
| Product | tert-Butyl 4-((4-(5-amino-1H-indol-1-yl)thiazol-2-yl)oxy)-piperidine-1-carboxylate | HCID 67616897 | — |
Reaction Steps
The title compound was prepared by following the similar procedure as described in Intermediate-27 using tert-butyl 4((4-bromothiazol-2-yl)oxy)piperidine-1-carboxylate and tert-butyl 1H-indol-5-ylcarbamate; MS: 415.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000175B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-f328571a1a484a539f8422c25a2aa829 |
| Source note | uspto-grants-2015_04 |