HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Difluorobenzaldehyde → HCID 69433288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| Reactant | HCID 11752390 | HCID 11752390 | — |
| Reactant | HCID 69431247 | HCID 69431247 | — |
| Product | HCID 69433288 | HCID 69433288 | — |
Reaction Steps
From (2S,4R)-2-azidomethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester was prepared via (2S,4R)-2-aminomethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester [as light brown foam, MS: 475 (MH+)] and further reaction with 2,5-difluoro benzaldehyde analogously to reductive amination gave (2S,4R)-2-[(2,5-difluoro-benzylamino)-methyl]-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester as colorless oil MS: 601 (MH+) which was treated according to trityl cleavage (method 5) to give (2S,4R)-2-[(2,5-difluoro-benzylamino)-methyl]-4-mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester as colorless liquid MS: 359 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790860B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-92fb198b04cc4f3e936636f06922f613 |
| Source note | uspto-grants-2004_09 |