HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate → (4R)-1-{3-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-5-chloro-2-oxo-2,3-dihydro-1H-indol-3-yl}-4-hydroxy-N,N-dimethy l-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate | HCID 67429482 | — |
| Reactant | 3-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-5-chloro-3-hydroxy-1,3-dihydro-2H-indol-2-one | HCID 67429824 | — |
| Product | (4R)-1-{3-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-5-chloro-2-oxo-2,3-dihydro-1H-indol-3-yl}-4-hydroxy-N,N-dimethy l-L-prolinamide | HCID 67428574 | — |
Reaction Steps
With 1.64 g of the compound obtained in Step 237-3 and (4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetate (5.67 mmol) as starting materials, respectively 901 mg (Isomer A: colorless solid) and 288 mg (Isomer B: colorless amorphous) of two species of diastereoisomers of the title compound were obtained by a similar method to Step 28-2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030499B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-c2f48a3c9bd8487e9a7740c088337f5f |
| Source note | uspto-grants-2011_10 |