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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912359Generated: October 31, 2026

2-Pyridinemethanamine → HCID 67385191, compound

https://huagongshe.com/reaction/912359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridinemethanamineHCID 19509—
Reactant4-(4-{2-[Bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-yl)-benzoic acidHCID 59244887—
ProductHCID 67385191HCID 67385191174.6%

Reaction Steps

Using 4-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-benzoic acid (60.0 mg, 0.0909 mmol) obtained in Step A in Example 1-D-19 and 2-(aminomethyl)pyridine (18.4 μl, 0.182 mmol) instead of 3-(aminomethyl)pyridine, amidation was carried out in the same manner as Step B in Example 1-D-19, to obtain a crude product of 4-[4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl]-N-pyridin-2-ylmethyl-benzamide as a brown solid (119 mg), and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-282) as a yellow powder (41.8 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-f56a6b9b86014ac68f9a1b00d26c3ee2
Source noteuspto-grants-2011_09