HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3S,4R)-4-benzyloxycarbonylamino-piperidine-3-carboxylic acid ethyl ester → (3S,4R)-4-benzyloxycarbonylamino-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-piperidine-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3S,4R)-4-benzyloxycarbonylamino-piperidine-3-carboxylic acid ethyl ester | HCID 66746417 | — |
| Reactant | (7-Methoxy-quinoxalin-2-ylsulfanyl)-acetaldehyde | HCID 86662002 | — |
| Product | (3S,4R)-4-benzyloxycarbonylamino-1-[2-(7-methoxy-quinoxalin-2-ylsulfanyl)-ethyl]-piperidine-3-carboxylic acid ethyl ester | HCID 66747494 | — |
Reaction Steps
The title compound is prepared as an off-white solid (232 mg, 70% yield) following Scheme 3 and in analogy to Example 35 using (3S,4R)-4-benzyloxycarbonylamino-piperidine-3-carboxylic acid ethyl ester (200 mg, 0.63 mmol, 1.0 eq) (prepared according to procedures described in WO2005/066176) and (7-methoxy-quinoxalin-2-ylsulfanyl)-acetaldehyde (158 mg, 0.63 mmol 1.0 eq) as starting materials.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716280B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-e623d6b501dc4c1f815f2d4862b2f61d |
| Source note | uspto-grants-2014_05 |