HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → (R)-methyl 5-bromo-1-((5-fluorothiazol-2-yl)carbamoyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 5-Fluoro-1,3-thiazol-2-amine hydrochloride | HCID 11858931 | — |
| Reactant | (R)-t-butyl 5-bromospiro[indoline-3,3'-pyrrolidine]-1'-carboxylate | HCID 90449881 | — |
| Product | (R)-methyl 5-bromo-1-((5-fluorothiazol-2-yl)carbamoyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylate | HCID 90449714 | — |
Reaction Steps
The captioned compound was obtained in the form of a white solid by performing the same reactions and/or treatments as those in Examples 1, 2, and 3, with the exceptions that (R)-t-butyl 5-bromospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate was used instead of t-butyl 5-bromospiro[indoline-3,3′-pyrrolidine]-1′-carboxylate, that 2-amino-5-fluorothiazole hydrochloride was used instead of 2-amino-5-chlorothiazole hydrochloride, and that methyl chloroformate was used instead of acetyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921576B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-170f33281ebb453cb6c686a2af97b8fe |
| Source note | uspto-grants-2014_12 |