Reaction equation
[NH2:1][CH2:2][CH2:3][CH:4]1[CH2:7][N:6]([CH:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:5]1.[C:21]([O:25][C:26](NCC1CN(C(C2C=CC=CC=2)C2C=CC=CC=2)C1)=[O:27])([CH3:24])([CH3:23])[CH3:22]>>[C:21]([O:25][C:26]([NH:1][CH2:2][CH2:3][CH:4]1[CH2:7][N:6]([CH:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:5]1)=[O:27])([CH3:24])([CH3:23])[CH3:22]Participants
3
Procedure
The title compound was prepared from 3-aminoethyl-1-benzhydryl azetidine according the procedure for 3-(N-tert-butyloxycarbonylaminomethyl)-1-benzhydryl azetidine, in a yield of 6.5 g (95%).
Sources & evidence
- ORD record
- ord-31c19a2463c1476fbe9eec12b7d3445c
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05602253
Linked notes
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