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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112766Generated: November 3, 2026

Cyclopropanecarbonyl chloride → HCID 69000631, compound

https://huagongshe.com/reaction/2112766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
Reactant2-Chloro-4-fluorobenzylamineHCID 139909—
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant2,4-Dichloro-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine--hydrogen chloride (1/1)HCID 45789965—
ReactantHCID 58731662HCID 58731662—
ProductHCID 69000631HCID 69000631—

Reaction Steps

From 2,4-dichloro-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine hydrochloride prepared according to Reference Example 1 and cyclopropylcarbonyl chloride, 2,4-dichloro-6-cyclopropylcarbonyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine was prepared in the same way as Process Step 1 of Example 1. Further, 2,4-dichloro-6-cyclopropylcarbonyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine was allowed to sequentially react with 2-chloro-4-fluorobenzylamine and N-(2-aminoethyl)(tert-butoxy)carboxamide in the same way as Process Steps 2 and 3 of Example 1, to yield 4-(2-chloro-4-fluorobenzylamino)-6-cyclopropylcarbonyl-2-(2-tert-butoxycarbonylaminoethylamino)-5,6,7,8-tetrahydropyrido [4,3-d]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524852B2
Source datasetuspto-grants-2009_04
ORD IDord-a5fb15b2d516469cb2f70d179a59b69f
Source noteuspto-grants-2009_04