HCID 54034664, compound → HCID 19849116, compound

HRID 1608321Notes

Reaction equation

HRID 1608321 reaction equation
C[O:2][C:3](=O)[CH2:4][NH:5][C:6]1[CH:11]=[C:10]([O:12][CH2:13][CH2:14][CH2:15][CH2:16][C:17]2[N:21]([CH:22]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)[N:20]=[N:19][N:18]=2)[CH:9]=[CH:8][C:7]=1[N+:28]([O-])=O>[Pd].C(O)C>[CH:22]1([N:21]2[C:17]([CH2:16][CH2:15][CH2:14][CH2:13][O:12][C:10]3[CH:11]=[C:6]4[C:7](=[CH:8][CH:9]=3)[NH:28][C:3](=[O:2])[CH2:4][NH:5]4)=[N:18][N:19]=[N:20]2)[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]1

Participants

4

Procedure

N-[5-{4-(1-cyclohexyl tetrazole-5-yl) butoxy}-2-nitropheny] amino acetic acid methyl ester 1.9 g (4.4 mM) and 10% Pd/C catalyst 1.9 g were added to ethanol 500 ml.

Sources & evidence

ORD record
ord-1a319c648e374e48b0bc91213125d2f9
Source dataset
uspto-grants-1989_09
Patent number
US04870175

Reaction notes

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