2-Ethoxy-malonic acid monoethyl ester → HCID 58972482, compound

HRID 31010Notes

Reaction equation

HRID 31010 reaction equation
[NH2:1][C@@H:2]1[C:8](=[O:9])[N:7]([CH2:10][CH2:11][O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:6]2[CH:20]=[CH:21][CH:22]=[CH:23][C:5]=2[C:4]2[CH:24]=[CH:25][CH:26]=[CH:27][C:3]1=2.[CH2:28]([O:30][C:31](=[O:39])[CH:32]([O:36][CH2:37][CH3:38])[C:33](O)=[O:34])[CH3:29]>>[CH2:28]([O:30][C:31](=[O:39])[CH:32]([O:36][CH2:37][CH3:38])[C:33]([NH:1][C@@H:2]1[C:8](=[O:9])[N:7]([CH2:10][CH2:11][O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:6]2[CH:20]=[CH:21][CH:22]=[CH:23][C:5]=2[C:4]2[CH:24]=[CH:25][CH:26]=[CH:27][C:3]1=2)=[O:34])[CH3:29]

Participants

3

Procedure

Using (S)-7-amino-5-(2-benzyloxy-ethyl)-5H,7H-dibenzo[b,d]azepin-6-one and 2-ethoxy-malonic acid monoethyl ester, the title compound was prepared in the same manner as described for example 1c. Colorless oil (94%). MS: m/e=517(M+H+).

Sources & evidence

ORD record
ord-37cf8da127ef4f3b892201f90b8210c9
Source dataset
uspto-grants-2008_09
Patent number
US07425551B2

Reaction notes

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