HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21476957, compound → HCID 21476970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21476957 | HCID 21476957 | — |
| Reactant | HCID 21476964 | HCID 21476964 | — |
| Product | HCID 21476970 | HCID 21476970 | — |
Reaction Steps
5-Benzyloxy-1-(2-carboxymethoxy-4-methoxybenzyl)-3-(3,4-methylenedioxyohenyl)indole-2-carboxylic acid. The title compound was prepared by alkylation of ethyl 5-benzyloxy-3-(3,4-methylenedioxyphenyl)indole-2-carboxylate with 2-carboethoxymethoxy-4-methoxybenzyl chloride followed by saponification using methods previously described in examples 1c and 1d; m.p. 182°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686481 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-f73d0a91171641aa9de0da896c465804 |
| Source note | uspto-grants-1997_11 |