HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079817Generated: October 30, 2026
2-Naphthalenecarboxaldehyde → Ethyl 2-(5-naphthalen-2-ylmethylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)pyrimidine-5-carboxylate
https://huagongshe.com/reaction/2079817
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl 2-hexahydropyrrolo[3,4-c]pyrrol-2(1H)-ylpyrimidine-5-carboxylate | HCID 59367682 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(5-naphthalen-2-ylmethylhexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)pyrimidine-5-carboxylate | HCID 59367601 | 99% |
Reaction Steps
To a solution of ethyl 2-hexahydropyrrolo[3,4-c]pyrrol-2(1H)-ylpyrimidine-5-carboxylate (0.187 g, 0.71 mmol) in DCE (2 ml) was added 2-naphthaldehyde (0.205 g, 1.31 mmol) and sodium triacetoxyborohydride (0.274 g, 1.25 mmol). The mixture was stirred for 3 h, then poured into DCM (100 ml). Sat. NaHCO3 (100 ml) was added, and extracted with further DCM (100 ml). The combined organic extracts were dried (MgSO4), concentrated and purified by flash column chromatography to yield the title compound (0.266 g, 99%). 1H NMR (300 MHz, CDCl3) δ: 1.39 (3H, t, J=6.9 Hz), 2.59 (2H, d, J=6.9 Hz), 2.73-2.90 (2H, m), 2.94-3.10 (2H, m), 3.67 (2H, d, J=11.7 Hz), 3.82 (2H, s), 3.90 (2H, dd, J=8.1, 12 Hz), 4.37 (2H, q, J=7.2 Hz), 7.41-7.43 (3H, m), 7.74 (1H, s), 7.76-7.89 (3H, m), 8.88 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932246B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-e06411dd06744f6babea7f125f036faf |
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| Source note | uspto-grants-2011_04 |
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