HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160349Generated: October 26, 2026
Diisopropylethylamine → HCID 58737501, compound
https://huagongshe.com/reaction/1160349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(p-Chlorophenyl)cyclobutanecarboxylic acid | HCID 602761 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | Methyl azetidine-3-carboxylate hydrochloride | HCID 21100040 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58737501 | HCID 58737501 | 70.6% |
Reaction Steps
To a stirred solution of azetidine-3-carboxylic acid methyl ester hydrochloride (762 mg, 4.60 mmoles) and 1-(4-chloro-phenyl)-cyclobutane carboxylic acid (2.09 g, 9.90 mmoles) in anhydrous DCM (20 mL) was added di-isopropyl ethyl amine (4.6 mL, 26.4 mmoles) dropwise. After completion of addition solid PyBroP (4.63 g, 9.94 mmoles) was added to the stirring reaction mixture. The reaction mixture continued stirring at RT for 10 h and was quenched with water. The aqueous layer was extracted with EtOAc (3×20 mL). Combined organic layers were dried over Na2SO4 and concentrated to yield an oil. This crude material was purified using silica gel chromatography (9:1 hexanes:EtOAc-1:1 hexane:EtOAc) to yield the desired amide (1.0 g, 65%). 1H NMR (300 MHz, CDCl3): δ 7.38-7.29 (m, 4H), 4.16 (m, 2H), 3.88 (m, 1H), 3.72 (s, 3H), 3.31-1.63 (m, 8H). LRMS: M+309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816375B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-f1d4ba7816bf4696a9e94429f41d858e |
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| Source note | uspto-grants-2010_10 |
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