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 | US07189756B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-ee036ecdb2af4db6b99728b7c577d3c5 |
| Source note | uspto-grants-2007_03 |