129822-41-9

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 95-69-2 4-chloro-2-methylbenzeneamine 

Downstream Products

• 1263300-11-3 C₁₇H₂₄ClNO₃ 
• 1263299-48-4 tert-butyl [4-chloro-2-(4-methyl-2-oxopentyl)phenyl]carbamate 
• 129822-48-6 tert-butyl 5-chloro-1H-indole-1-carboxylate 
• 17630-75-0 5-chloro-indolin-2-one 
• 866405-01-8 5-chloro-2-propyl-1H-indole 
• 573716-57-1 [4-chloro-2-(3-methyl-2-oxo-butyl)-phenyl]-carbamic acid tert-butyl ester 
• 866405-03-0 [4-chloro-2-(2-oxo-pentyl)-phenyl]-carbamic acid tert-butyl ester 
• 866405-02-9 [4-chloro-2-(2-oxo-butyl)-phenyl]-carbamic acid tert-butyl ester 
• 457622-18-3 3-(2-amino-5-chlorophenyl)-1-propanol 
• 164226-33-9 tert-butyl 2-tert-butoxycarbonylamino-4-chlorophenyl acetate 
• 138343-87-0 2-(N-tert-butoxycarbonyl)amino-5-chlorophenylacetic acid 

Relevant academic research and scientific papers

2-Alkyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoles as novel 5-HT 6 receptor agonists

A series of 2-alkyl-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoles were synthesized and evaluated for their 5-HT6 activity. The most potent agonist in this series was 5-chloro-2-methyl-3-(1,2,3,6-tetrahydropyridin-4-yl)- 1H-indole with an ICsub

1H-INDOLE-3-ACETIC ACID HYDRAZIDE SPLA2 INHIBITORS

A class of novel 1H-indole-3-acetic acid hydrazides is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids (e.g., arachidonic acid) for treatment of conditions such as septic shock

Preparation of indoles and oxindoles from N-(tert-butoxycarbonyl)-2-alkylanilines

Treatment of dilithiated N-(tert-butoxycarbonyl)anilines 1 with dimethylformamide or carbon dioxide furnishes intermediates 3, 5, that are easily converted to N-(tert-butoxycarbonyl)indoles 4 and oxindoles (indol-2(3H)-ones, 7), respectively. Condensation of dilithiated 1 with N-methoxy-N-methylamides provides ketones 9 which are cyclized upon trifluoroacetic acid treatment to either 2-substituted 1-(tert-butoxycarbonyl)indoles 10 or 2-substituted indoles 11 depending on the reaction time. This general methodology has been applied to efficient synthesis of 1,2-alkyl-bridged indoles 12, 1,3,4,5-tetrahydrobenz[c,d]indole (16), 2a,3,4,5-tetrahydrobenz[c,d]indol-2(1H)-one (18), and 1-(tert-butoxycarbonyl)1H-pyrrolo[2,3-b]pyridine (21).