HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801554Generated: October 25, 2026
Sodium Bicarbonate → HCID 178483045, compound
https://huagongshe.com/reaction/1801554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Dimethylamino)-5-pyrimidinecarbaldehyde | HCID 795544 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-morpholin-4-yl-6-piperidin-4-yl-1H-pyrimidin-4-one;hydrochloride | HCID 178479622 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178483045 | HCID 178483045 | 69% |
Reaction Steps
2-Morpholin-4-yl-6-piperidin-4-yl-pyrimidin-4-ol, hydrochloride salt (0.16 g, 0.47 mmol), 2-dimethylamino-pyrimidine-5-carboxaldehyde (86 mg, 0.57 mmol), and one drop of acetic acid were mixed in dry dichloromethane (10 mL) for 3 hours at room temperature. Sodium cyanoborohydride (88 mg, 1.42 mmol) was added and the mixture stirred for 3 days. The mixture was poured into saturated sodium bicarbonate solution and extracted with dichloromethane (3×50 mL). The material was purified on silica gel, eluting with 10% methanol in dichloromethane to provide 6-[1-(2-Dimethylaminopyrimidin-5-ylmethyl)-piperidin-4-yl]-2-morpholin-4-yl-pyrimidin-4-ol (Compound IIa, 0.11 g, 69% yield) as a white solid. CHN Analysis: Calculated for C20H29N7O2: 60.13 C, 7.32 H, 24.54 N; found 57.31 C, 7.11 H, 23.68 H. Bestfit is C20H29N7O2+1H2O; 57.54 C, 7.48 H, 23.48 N. 1H NMR (300 MHz, CDCl3/CD3OD/TMS): δ=8.26 (s, 2H), 5.65 (s, 1H), 3.85-3.60 (m, 8H), 3.42 (m, 2H), 3.19 (s, 6H), 3.15-2.85 (m, 3H), 2.40-2.00 (m, 2H), 2.18-1.60 (m, 4H). 13C NMR (75 MHz, CDCl3/CD3OD/TMS): δ=173.66, 161.63, 158.91, 153.90, 116.63, 98.76, 66.56, 57.62, 53.12, 44.94, 43.65, 37.48, 30.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349833B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-73628b30845349a6a38e2bab905a0de9 |
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| Source note | uspto-grants-2013_01 |
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