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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291001Generated: October 30, 2026

t-Butyl 4-[(6-cyano-1-methyl-2-indolyl)carbonylamino]phenoxyacetate → t-Butyl 4-[(6-amidino-1-methyl-2-indolyl)carbonylamino]phenoxyacetate

https://huagongshe.com/reaction/1291001

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl 4-[(6-cyano-1-methyl-2-indolyl)carbonylamino]phenoxyacetateHCID 10763801—
Reactant6-cyano-1-methyl-1H-indole-2-carboxylic acidHCID 10798077—
ReactantTert-butyl 2-(4-aminophenoxy)acetateHCID 22060435—
Productt-Butyl 4-[(6-amidino-1-methyl-2-indolyl)carbonylamino]phenoxyacetateHCID 10598318—

Reaction Steps

In the same manner as in Example 1 (2), 6-cyano-1-methyl-2-indolcarboxylic acid (52 mg, 0.26 mmol) and t-butyl 4-aminophenoxyacetate (63 mg, 0.29 mmol) were condensed to quantitatively give 109 mg of t-butyl 4-[(6-cyano-1-methyl-2-indolyl)carbonylamino]phenoxyacetate as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753670
Source datasetuspto-grants-1998_05
ORD IDord-67e2bbf8f4814ee4a3e4fcb7022d2193
Source noteuspto-grants-1998_05