HCID 69370037, compound → HCID 69370287, compound

HRID 1816807Notes

Reaction equation

HRID 1816807 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]([C:12]2[CH:20]=[C:19]3[C:15]([C:16]([CH:29]=[CH:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)=[N:17][N:18]3COCC[Si](C)(C)C)=[CH:14][CH:13]=2)=[O:11])[CH:7]=[CH:8][CH:9]=1)([O-])=O.NC1C=C(C(C2C=C3C(C(C=CC4C=CC=CC=4)=NN3COCC[Si](C)(C)C)=CC=2)=O)C=CC=1>>[NH2:1][C:4]1[CH:5]=[C:6]([C:10]([C:12]2[CH:20]=[C:19]3[C:15]([C:16]([CH:29]=[CH:30][C:31]4[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=4)=[N:17][NH:18]3)=[CH:14][CH:13]=2)=[O:11])[CH:7]=[CH:8][CH:9]=1

Participants

3

Reactant 2

HCID 69370037HCID 69370037, compoundHCID 69371190HCID 69371190, compound

Product 1

HCID 69370287HCID 69370287, compound

Procedure

(3-Nitrophenyl) (3-styryl-1-[2-(trimethyl-silanyl)ethoxymethyl]-1H-indazol-6-yl)-methanone was converted to (3-amino-phenyl)-{3-styryl-1-[2-(trimethyl-silanyl) ethoxymethyl]-1H-indazol-6-yl}-methanone as described in Example 11, step (iv) (102 mg, 84%). LCMS (ESI) [M+H]/z Calc'd 340, found 340.

Sources & evidence

ORD record
ord-65458197b3874a5bbc817570fcf8a81e
Source dataset
uspto-grants-2005_04
Patent number
US06884890B2

Reaction notes

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