HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244158Generated: October 27, 2026
1,1'-Carbonyldiimidazole → HCID 178501155, compound
https://huagongshe.com/reaction/244158
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(Methoxycarbonyl)cyclohexane-1-carboxylic acid | HCID 296850 | — |
| Reactant | (3-Chloropyrazin-2-yl)methanamine dihydrochloride | HCID 42609650 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178501155 | HCID 178501155 | — |
Reaction Steps
A THF (370 mL) solution of 4-(methoxycarbonyl)cyclohexanecarboxylic acid (15.14 g, 81.30 mmol) and CDI (13.18 g, 81.30 mmol) was placed under a nitrogen atmosphere and stirred at 60° C. for 4 h. The reaction mixture was cooled to r.t., then, (3-chloropyrazin-2-yl)methylamine bis-hydrochloride salt (16.00 g, 73.91 mmol) and DIPEA (31.52 g, 244.00 mmol, 42.5 mL) was added. After stirring at 60° C. for 20 h, the reaction was concentrated in vacuo. The crude reaction mixture was purified by a silica gel glass column chromatography (eluted with 3:2 DCM/EtOAc) to obtain the pure desired product as a slightly yellowish creamy white powder; 1H NMR (CDCl3, 400 MHz) δ 1.43-1.65 (m, 4H), 2.01-2.14 (m, 4H), 2.25 (tt, J=12.0, 3.6 Hz, 1H), 2.34 (tt, J=11.6, 3.2 Hz, 1H), 3.68 (s, 3H), 4.70 (d, J=4.4 Hz, 2H), 6.81 (s, br, —NH), 8.32-8.36 (m, 1H), 8.46 (d, J=2.4 Hz, 1H); MS (ES+): m/z 312.17/314.12 (84/32) [MH+]; HPLC: tR=2.44 min (OpenLynx, polar—5 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653268B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-828d95e075ca490e9589b03499e6ff4b |
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| Source note | uspto-grants-2014_02 |
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