HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413031Generated: October 30, 2026
3-(Phenylsulfonyl)propanoic acid → Diisopropylcarbodiimide
https://huagongshe.com/reaction/413031
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(Phenylsulfonyl)propanoic acid | HCID 555252 | — |
| Reactant | HCID 17751339 | HCID 17751339 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diisopropylcarbodiimide | HCID 12734 | — |
| Product | 1-[Bis(4-chlorophenyl)methyl]azetidin-3-ylamine | HCID 21896598 | — |
Reaction Steps
By carrying out the operation according to the procedure of Example 31, starting with 58.5 mg of 3-phenylsulfonylpropionic acid, 26.4 mg of hydroxybenzotriazole in solution in 0.5 cm3 of dimethylformamide, 0.0302 cm3 of diisopropylcarbodiimide, a solution of 30 mg of 1-[bis(4-chlorophenyl)methyl]azetidin-3-ylamine in 0.5 cm3 of anhydrous dichloromethane, and 3 cm3 of anhydrous dichloromethane, N-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-4-methanesulfonylbenzamide is obtained in the form of a lacquer [1H NMR spectrum (300 MHz, CDCl3, δ in ppm): 2.71 (t, J=7.5 Hz: 2H) 2.86 (mt: 2H); from 3.40 to 3.55 (mt: 4H); 4.26 (s: 1H); 4.45 (mt: 1H); 6.22 (broad d, J=7.5 Hz: 1H); from 7.20 to 7.35 (mt: 8H); 7.59 (broad t, J=7.5 Hz: 2H); 7.69 (tt, J=7.5 and 1.5 Hz: 1H); 7.93 (broad d, J=7.5 Hz: 2H)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566356B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-b2dbd4a2ba954123a532088c9a4bb0d2 |
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| Source note | uspto-grants-2003_05 |
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