HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912240Generated: November 1, 2026
2-Morpholinoethylamine → HCID 67385545, compound
https://huagongshe.com/reaction/912240
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 4-(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 acid | HCID 59244887 | — |
| Reactant | HCID 59244923 | HCID 59244923 | — |
| Product | HCID 67385545 | HCID 67385545 | 99.9% |
Reaction Steps
Using 3-(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 (69.6 mg, 0.105 mmol) obtained in Step A in Example 1-D-53 instead 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)-benzoic acid, and N-(2-aminoethyl)morpholine (27.5 mg, 0.211 mmol) instead of 3-(aminomethyl)pyridine, in the same manner as Step B in Example 1-D-19, amidation was carried out, to obtain a crude product of 3-[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-(2-morpholin-4-yl-ethyl)-benzamide as a yellow solid (81.0 mg), and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-123) as a yellow powder (34.2 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022205B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-8767f18acd5b4248b46bea618bb08df4 |
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| Source note | uspto-grants-2011_09 |
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