HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 4-hydroxypiperidine-1-carboxylate → 4-(Thiazol-2-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | HCID 178527881 | HCID 178527881 | — |
| Product | 4-(Thiazol-2-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester | HCID 18538907 | — |
Reaction Steps
By a similar manner to Reference Example 35, 1-tert-butoxycarbonyl-4-hydroxypiperidine (1.01 g, 5.0 mmol) was reacted with 2-mercaptothiazole (0.70 g, 6.0 mmol) to give the titled compound as pale yellow oily substance (1.33 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348324B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-1c56dbc6b1dd42eb9ea2b26d8dd73c0c |
| Source note | uspto-grants-2008_03 |