HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424633Generated: November 1, 2026
Diisopropylethylamine → HCID 66953826, compound
https://huagongshe.com/reaction/1424633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Isocyanatoadamantane | HCID 12882630 | — |
| Reactant | HCID 58137314 | HCID 58137314 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66953826 | HCID 66953826 | 97% |
Reaction Steps
To a stirred solution of 3-allyl-7-chloro-3H-spiro[isobenzofuran-1,4′-piperidine] (0.0190 g), and DIEA (0.5 mL) in CH2Cl2 (2 mL) was added 2-adamantyl isocyanate (0.0138 g, 0.0778 mmol) at rt. After 19 h, the solvents were removed in vacuo and the residue was purified by reversed-phase HPLC (Phenomenex® Luna 5μ C18(2) 100A, 250×21.20 mm, 5 micron, 70%→90% CH3CN/H2O, 0.1% CF3COOH over 8 min and then 90% CH3CN/H2O, 0.1% CF3COOH over 4 min, flow rate 25 mL/min) to afford N-(2-adamantyl)-3-allyl-7-chloro-3H-spiro[isobenzofuran-1,4′-piperidine]-1′-carboxamide (0.0220 g, 97%). LC-MS Method 1 tR=2.33 min, m/z 443, 441 (MH+); 1H NMR (400 MHz, CDCl3) δ=7.24-7.20 (m, 2H), 7.09-7.05 (m, 1H), 5.87-5.77 (m, 1H), 5.25 (t, J=5.7 Hz, 1H), 5.15-5.08 (m, 2H), 3.98 (br s, 1H), 3.94-3.88 (m, 2H), 136-3.28 (m, 2H), 2.66-2.38 (m, 4H), 1.95-1.25 (m, 16H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927715B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-c69249f512284d6a98ac4024f123ccba |
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| Source note | uspto-grants-2015_01 |
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