HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272934Generated: October 25, 2026
Diisopropylethylamine → HCID 59837431, compound
https://huagongshe.com/reaction/272934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2-Dimethylpyrrolidine | HCID 414773 | — |
| Reactant | HCID 23091704 | HCID 23091704 | — |
| Reactant | 1-[4-(3-Bromo-propoxy)-phenyl]-cyclohexanecarbonitrile | HCID 59837504 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 59837431 | HCID 59837431 | 17% |
Reaction Steps
A (1:3) mixture of 1-[4-(3-bromo-propoxy)-phenyl]-cyclohexanecarbonitrile and 1-[4-(3-chloro-propoxy)-phenyl]-cyclohexanecarbonitrile (150 mg, 0.54 mmol), N,N-diisopropylethylamine (188 μL, 1.08 mmol) and 2,2-dimethyl-pyrrolidine (131 mg, 1.08 mmol) in NMP (0.5 mL) was heated at 180° C. in the microwave (Smith Personal Synthesiser) for 600 seconds. The reaction mixture was quenched with water (15 mL) and extracted with ethyl acetate (2×15 mL), dried over Na2SO4, filtered and concentrated in vacuo. The compound was purified by column chromatography on Biotage® silica gel, eluting with dichloromethane:methanol:ammonia, 98:2:0.2 to 95:5:0.5 to give the title compound as a brown oil (31 mg, 17%). 1H NMR (400 MHz, CDCl3) δ7.38 (d, 2H), 6.90 (d, 2H), 4.04 (t, 2H), 2.78 (t, 2H), 2.54 (t, 2H), 2.16-2.12 (m, 2H), 1.94 (pentet, 2H), 1.90-1.64 (m, 11H), 1.20-1.34 (m, 1H), 0.98 (s, 6H); HRMS (ESI+) 341.2588 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456164B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-99f121676a1e4897ae779a4d906ebbbd |
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| Source note | uspto-grants-2008_11 |
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