Cyclopentylamine → 3-chloro-N-cyclopentylbenzamide
Reaction equation
[CH:1]1([NH2:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=1)[C:11](Cl)=[O:12]>>[Cl:7][C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=1)[C:11]([NH:6][CH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:12]Participants
3
Procedure
Employing 0.16 g (1.9 mmol) of cyclopentylamine and 0.51 g, (2.9 mmol) of 3-chloro-benzoyl chloride in the procedure described above and elution with CHCl3/MeOH/Et3N (9.8:0.1:0.1) gave white crystals in 92% yield).
Workup
- washelution with CHCl3/MeOH/Et3N (9.8:0.1:0.1)
- customgave white crystals in 92% yield)
Sources & evidence
- ORD record
- ord-542791f0f382422f960f4c5e087ed867
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975288B2
Reaction notes
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