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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093898Generated: November 1, 2026

tert-butyl (3R)-3-aminopiperidine-1-carboxylate → (R)-3-{[4-(2-Cyclopropylmethoxy-5-fluoro-4-methoxy-phenyl)-5H-pyrrolo[3,2-d]pyrimidine-7-carbonyl]-amino}-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2093898

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
Reactant4-(2-Cyclopropylmethoxy-5-fluoro-4-methoxy-phenyl)-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acidHCID 66866404—
Product(R)-3-{[4-(2-Cyclopropylmethoxy-5-fluoro-4-methoxy-phenyl)-5H-pyrrolo[3,2-d]pyrimidine-7-carbonyl]-amino}-piperidine-1-carboxylic acid tert-butyl esterHCID 66867767—

Reaction Steps

Starting from 4-(2-Cyclopropylmethoxy-5-fluoro-4-methoxy-phenyl)-5H-pyrrolo[3,2-d]pyrimidine-7-carboxylic acid (example A80) and (R)-3-amino-piperidine-1-carboxylic acid tert-butyl ester the title compound is obtained as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445501B2
Source datasetuspto-grants-2013_05
ORD IDord-9408e967aebe43119a31b59d1d61bf4d
Source noteuspto-grants-2013_05