HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidine → HCID 11609449, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidine | HCID 10444 | — |
| Reactant | 2-(2-Bromoethyl)pyridine | HCID 12913858 | — |
| Reactant | HCID 58745510 | HCID 58745510 | — |
| Product | HCID 11609449 | HCID 11609449 | — |
Reaction Steps
This material was obtained as described in example 34 from the opposite enantiomer (3S, 4R)-4-amino-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester, thiazolidine and 2-(2-bromo-ethyl)-pyridine (synthesized according to Synthesis, 5, 1987, 452-455). Yellow oil. MS (ESI): 321.4 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07683079B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-59add753df0f4a13b38eff956947b61d |
| Source note | uspto-grants-2010_03 |