HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989872Generated: October 25, 2026
Diisopropylamine → (1,1'-Biphenyl)-2-carboxamide
https://huagongshe.com/reaction/1989872
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | o-Phenylbenzoic acid | HCID 70357 | — |
| Reactant | 4-[1-(Phenylmethyl)-4-piperidinyl]-benzenamine | HCID 22499396 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1,1'-Biphenyl)-2-carboxamide | HCID 83254 | 253.5% |
Reaction Steps
2-Biphenylcarboxylic acid (0.25 mol) was dissolved in DCM (500 ml) and DMF (0.5 ml). Thionyl chloride (0.51 mol) was added dropwise. The mixture was stirred and refluxed for 1 hour under nitrogen flow. The solvent was evaporated. DCM (500 ml) was added twice. The solvent was evaporated twice. The residue was dissolved in DCM (200 ml) and then added dropwise at 0° C. to a mixture of 4-[1-(phenylmethyl)-4-piperidinyl]-benzenamine (0.25 mol) and N-(1-methylethyl)-2-propanamine (0.75 mol) in DCM (800 ml). The mixture was brought to room temperature and then stirred at room temperature overnight under nitrogen flow. The mixture was washed three times with water (800 ml). The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 125 g of [1,1′-biphenyl]-2-carboxamide, N-[4-[1-(phenylmethyl)-4-piperidinyl]phenyl]-(intermediate 39).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642378B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-e652dd9fed5846eaa8cce00d70d967af |
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| Source note | uspto-grants-2010_01 |
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