HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-alanine → N-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-Nalpha-(9-fluorenylmethoxycarbonyl)-L-alanine amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-alanine | HCID 6364642 | — |
| Reactant | N-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amine | HCID 18460594 | — |
| Product | N-[2-(tert-butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]-Nalpha-(9-fluorenylmethoxycarbonyl)-L-alanine amide | HCID 86758402 | — |
Reaction Steps
N-[2-(tert-Butyldimethylsilyloxy)ethyl]-N-[[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl]amine (756 mg) and N-(9-fluorenylmethoxycarbonyl)-L-alanine (544 mg) were treated in the same manner as in Preparation Example 9 to obtain the title compound. Since this compound was unable to be isolated from impurities, it was used in the next reaction without purifying it as it is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06432957B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-e66b1104d77c49c6b953eb064b635d3f |
| Source note | uspto-grants-2002_08 |