Fmoc-Gly-OH → 7-Aminonimetazepam
反応式
C(NCC(O)=O)(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O.NC1C=C([N+]([O-])=O)C=CC=1C(C1C=CC=CC=1)=O.[NH2:41][C:42]1[CH:61]=[CH:60][C:45]2[N:46]([CH3:59])[C:47](=[O:58])[CH:48](C)[N:49]=[C:50]([C:51]3[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=3)[C:44]=2[CH:43]=1>>[NH2:41][C:42]1[CH:61]=[CH:60][C:45]2[N:46]([CH3:59])[C:47](=[O:58])[CH2:48][N:49]=[C:50]([C:51]3[CH:56]=[CH:55][CH:54]=[CH:53][CH:52]=3)[C:44]=2[CH:43]=1参加物
4
実験手順
This compound was prepared from Fmoc-glycine and 2-amino-4-nitro-benzophenone using the same procedure used for the enantiomers of 7-amino-1,3-dimethyl-5-phenyl-1H-benzo[e][1,4]diazepin-2(3H)-one. Chemical and physical characteristics of the intermediate and final compounds are reported:
出典と根拠
- ORDレコード
- ord-aa9f83a730a94bd3b1d4bad62f300f3c
- 出典データセット
- uspto-grants-2012_12