HuagongsheHuagongshe Chemistry Print Report · For research reference only
Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester → HCID 178515582, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester | HCID 66640668 | — |
| Reactant | HCID 178463708 | HCID 178463708 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178515582 | HCID 178515582 | 18% |
Reaction Steps
In a manner similar to the method described in example 1e, E/Z-6-chloro-3-(3-chloro-benzylidene)-2-oxo-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester prepared in example 1b (1.52 g, 3.8 mmol) was reacted 1-[2-[cis-4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyloxy]-5-chloro-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene (9.8 mmol) in toluene to give racemic(2′R, 3R, 4′S)-6-chloro-2′-[5-chloro-2-(cis-4-hydroxy-cyclohexyloxy)-phenyl]-4′-(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′(1H)-dione as a white solid (Yield 0.4 g, 18%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134001B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-c0f86f5cdae14945b2038eb473c0da8c |
| Source note | uspto-grants-2012_03 |