Реакция #51756

ord-4785ced226c74426bde033d537ae8572

Уравнение реакции

CC(C)(C)OC(=O)N1CCc2cc(SC#N)c(C(C)(C)C)cc21
6-tert-butyl-5-thiocyanato-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
O[C@H](CS)[C@H](O)CS
dithiothreitol
O=P([O-])([O-])[O-]
phosphate
→
CC(C)(C)OC(=O)N1CCc2cc(S)c(C(C)(C)C)cc21
title compound
CC(C)(C)OC(=O)N1CCc2cc(S)c(C(C)(C)C)cc21
6-tert-Butyl-5-mercapto-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester

Реактанты

CC(C)(C)OC(=O)N1CCc2cc(SC#N)c(C(C)(C)C)cc21
6-tert-butyl-5-thiocyanato-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester
O[C@H](CS)[C@H](O)CS
dithiothreitol
O=P([O-])([O-])[O-]
phosphate

Реагенты

Нет

Растворители

CCO
EtOH

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe crude product was used without any purification

Методика

The title compound was prepared according to General Method 14 using 6-tert-butyl-5-thiocyanato-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (prepared in Example KK; 2.0 g, 6.6 mmol), dithiothreitol (1.21 g, 7.9 mmol), EtOH (100 mL), and phosphate buffer (pH: 7.5, 10 mL). The crude product was used without any purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06852711B2uspto-grants-2005_02