HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912235Generated: November 1, 2026
1,3-Propanediamine, N1,N1,N3-trimethyl- → HCID 67385279, compound
https://huagongshe.com/reaction/912235
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N1,N1,N3-trimethyl- | HCID 78302 | — |
| Reactant | HCID 59244926 | HCID 59244926 | — |
| Product | HCID 67385279 | HCID 67385279 | 72.2% |
Reaction Steps
Using {5-[7-(6-chloro-pyridin-3-yl)-2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-pyrimidin-2-yl}-bis-(4-methoxy-benzyl)-amine (200 mg, 0.307 mmol) obtained in Step A in Example 1-D-48 and N,N,N′-trimethyl-1,3-propanediamine (67 μl, 0.46 mmol) instead of N,N,N′-trimethyl ethylenediamine, in the same manner as Step B in Example 1-D-48, amination was carried out, to obtain a crude product of N-[5-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-pyridin-2-yl]-N,N′,N′-trimethyl-propan-1,3-diamine as a pale yellow solid (162 mg), and then the PMB groups were removed according to the above Deprotection method 2, to obtain the desired compound (D-116) as a colorless powder (67 mg, 57%).
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-2b3acddf3fe148ebbb37d85cec509a03 |
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| Source note | uspto-grants-2011_09 |
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