HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902940Generated: October 30, 2026
Diisopropylcarbodiimide → HCID 69211444, compound
https://huagongshe.com/reaction/902940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 2-(4-Biphenyl)ethylamine | HCID 28210 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 69210030 | HCID 69210030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69211444 | HCID 69211444 | — |
Reaction Steps
To a solution of the compound of example 29 (200 mg, 0.41 mmol) and HOBt (66 mg, 0.49 mmol) in DMF (2 mL), were added 4-biphenylethylamine (124 mg, 0.62 mmol) and DIC (78 μL) respectively. The reaction mixture was stirred for 24 h at room temperature. The reaction mixture was partitioned between HCl (0.5N, excess) and ethyl acetate. The aqueous phase was extracted several times with ethyl acetate. The recombined organic layer was washed with brine, with a saturated sodium hydrogen carbonate solution, and again with brine. The solvent was evaporated following drying over sodium sulfate, and the crude was flashed using 30% ethyl acetate in hexanes. 1H-NMR (CDCl3, 400 MHz: 1.55(s, 9H); 1.41-1.57(m, 2H); 2.04-2.28(m, 6H); 2.54(m, 1H); 2.80(m, 2H); 3.45-3.55(m, 2H), 5.66(m, 1H); 7.19-7.57(m, 24H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365091B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-690e1d6201194304acee7a9d792a0534 |
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| Source note | uspto-grants-2008_04 |
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