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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043563Generated: October 25, 2026

2-cyclopropyl-1H-1,3-benzodiazole → 2-(1-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-ol

https://huagongshe.com/reaction/1043563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-cyclopropyl-1H-1,3-benzodiazoleHCID 1084419—
Reactant2-(1-((2-Chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-olHCID 58404970—
Product2-(1-((2-(2-cyclopropyl-1H-benzo[d]imidazol-1-yl)-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-olHCID 53377949—

Reaction Steps

Following General Procedure C, 2-cyclopropyl-benzimidazole and 2-(1-((2-chloro-4-morpholinopyrido[3,2-d]pyrimidin-6-yl)methyl)piperidin-4-yl)propan-2-ol from Example 8 were reacted to give 102. LCMS (MH+)=528.3. 1H-NMR (DMSO-d6): δ 8.19 (d, 1H), 8.03 (m, 1H), 7.89 (d, 1H), 7.44 (m, 1H), 7.23 (m, 2H), 4.56 (s, 4H), 4.01 (s, 1H), 3.83 (m, 4H), 3.74 (2, 2H), 2.94 (m, 3H), 1.99 (m, 2H), 1.67 (m, 2H), 1.29 (m, 2H), 1.16 (m, 3H), 1.08 (m, 2H), 1.04 (s, 6H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563540B2
Source datasetuspto-grants-2013_10
ORD IDord-f54a83855a73435b85c45760fc6aa369
Source noteuspto-grants-2013_10