HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Difluorobenzaldehyde → HCID 86584841, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| Reactant | HCID 69431427 | HCID 69431427 | — |
| Product | HCID 86584841 | HCID 86584841 | — |
Reaction Steps
(2S,4R)-2-aminomethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid benzyl ester and 2,5-difluorobenzaldehyde and subsequent cleavage of the trityl protecting group analogously to reductive amination and deprotection gave (2S,4R)-2-[(2,5-difluoro-benzylamino)-methyl]-4-mercapto-pyrrolidine-1-carboxylic acid benzyl ester as colorless oil, MS: 393 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790860B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-0c659fa1f0fc4a298ec8ee6a622b4471 |
| Source note | uspto-grants-2004_09 |