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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662773Generated: October 30, 2026

(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

https://huagongshe.com/reaction/1662773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4R)-4-hydroxy-N,N-dimethyl-L-prolinamide trifluoroacetateHCID 67429482—
Reactant3-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-methoxyphenyl]-5-chloro-3-hydroxy-1,3-dihydro-2H-indol-2-oneHCID 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-prolinamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-c2f48a3c9bd8487e9a7740c088337f5f
Source noteuspto-grants-2011_10