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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112767Generated: November 1, 2026

Tert-butyl 4-(2-pyrrolidin-1-ylacetyl)piperidinecarboxylate → 4-(N-tert-butoxycarbonyl-2-chloro-4-fluorobenzylamino)-6-cyclopropylcarbonyl-2-[4-(2-pyrrolidin-1-ylacetyl)piperidino]-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

https://huagongshe.com/reaction/2112767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-pyrrolidin-1-ylacetyl)piperidinecarboxylateHCID 23079654—
Reactant4-(N-tert-butoxycarbonyl-2-chloro-4-fluorobenzylamino)-2-chloro-6-cyclopropylcarbonyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidineHCID 86610787—
Product4-(N-tert-butoxycarbonyl-2-chloro-4-fluorobenzylamino)-6-cyclopropylcarbonyl-2-[4-(2-pyrrolidin-1-ylacetyl)piperidino]-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidineHCID 69002519—

Reaction Steps

In the same way as Example 92 mentioned later, 4-(N-tert-butoxycarbonyl-2-chloro-4-fluorobenzylamino)-6-cyclopropylcarbonyl-2-[4-(2-pyrrolidin-1-ylacetyl)piperidino]-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine was prepared from 4-(N-tert-butoxycarbonyl-2-chloro-4-fluorobenzylamino)-2-chloro-6-cyclopropylcarbonyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine prepared according to Process Step 1 and tert-butyl 4-(2-pyrrolidin-1-ylacetyl)piperidinecarboxylate prepared according to Reference Example 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524852B2
Source datasetuspto-grants-2009_04
ORD IDord-b3cc8527ea824b8f81854226d53a2a88
Source noteuspto-grants-2009_04