5-Methoxytryptamine → N5-[Amino(nitroimino)methyl]-N2-(diphenylacetyl)-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-ornithinamide

HRID 52584

反応式

HRID 52584 の反応式
[NH2:1][C:2](=[N:27][N+:28]([O-:30])=[O:29])[NH:3][CH2:4][CH2:5][CH2:6][C@H:7]([C:24]([OH:26])=O)[NH:8][C:9](=[O:23])[CH:10]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH3:31][O:32][C:33]1[CH:44]=[C:43]2[C:36]([NH:37][CH:38]=[C:39]2[CH2:40][CH2:41][NH2:42])=[CH:35][CH:34]=1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F>>[NH2:1][C:2](=[N:27][N+:28]([O-:30])=[O:29])[NH:3][CH2:4][CH2:5][CH2:6][C@@H:7]([C:24]([NH:42][CH2:41][CH2:40][C:39]1[C:43]2[C:36](=[CH:35][CH:34]=[C:33]([O:32][CH3:31])[CH:44]=2)[NH:37][CH:38]=1)=[O:26])[NH:8][C:9](=[O:23])[CH:10]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

参加物

4

実験手順

Prepared analogously to Example 5d) from (R)-N5 -[amino (nitroimino) methyl]-N2 -(diphenylacetyl)-ornithine, 5-methoxytryptamine and TBTU in a yield of 36% of theory.

出典と根拠

ORDレコード
ord-732e3adc46b94790b37139b1a76e39f3
出典データセット
uspto-grants-1997_04
特許番号
US05616620

関連ノート

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