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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062023Generated: October 27, 2026

2-[2-(tert-butyldimethylsilanyloxy)propyl]-4,6,7-trichloro-2H-indazole → 2-Amino-2-methyl-3-(4,6,7-trichloro-2H-indazol-2-yl)propionitrile

https://huagongshe.com/reaction/2062023

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[2-(tert-butyldimethylsilanyloxy)propyl]-4,6,7-trichloro-2H-indazoleHCID 66620175—
Reactant1-(4,6,7-Trichloro-2H-indazol-2-yl)propan-2-oneHCID 66620713—
Reactant2-Nitro-3,4,6-trichlorobenzaldehydeHCID 86625590—
Product1-(4,6,7-Trichloro-2H-indazol-2-yl)propan-2-oneHCID 66620713—
Product2-Amino-2-methyl-3-(4,6,7-trichloro-2H-indazol-2-yl)propionitrileHCID 6662089160%

Reaction Steps

2-Amino-2-methyl-3-(4,6,7-trichloro-2H-indazol-2-yl)propionitrile (0.16 g, 60%) was prepared using a procedure similar to that described in Example 1, part b, except starting from 1-(4,6,7-trichloro-2H-indazol-2-yl)propan-2-one (0.25 g). 1-(4,6,7-Trichloro-2H-indazol-2-yl)propan-2-one was prepared using a procedure similar to that described in Example 105 part c and d except starting from 2-[2-(tert-butyldimethylsilanyloxy)propyl]-4,6,7-trichloro-2H-indazole (1.4 g, 69%) that was prepared using a procedure similar to that described in Example 132 part a except starting from [2-(tert-butyldimethylsilanyloxy)propyl]-(2-nitro-3,4,6-trichlorobenzypamine (2.2 g). [2-(tert-Butyldimethylsilanyloxy)propyl]-(2-nitro-3,4,6-trichlorobenzypamine (2.2 g, 44%) was prepared using a procedure similar to that described in Example 105 part a except starting from 2-nitro-3,4,6-trichlorobenzaldehyde (3 g) that was prepared as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283475B2
Source datasetuspto-grants-2012_10
ORD IDord-14e18b20ecd64dc48ef136ae9438752d
Source noteuspto-grants-2012_10