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HRID 23265Erstellt: 23. Oktober 2026

1-Bromo-2,3-dichlorobenzene → (7bR,11aS)-N-(2,3-dichlorophenyl)-1,2,7b,8,9,10,11,11 a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amine

https://huagongshe.com/de/reaction/23265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2,3-dichlorobenzeneHCID 42066—
Edukttert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H) carboxylateHCID 86586437—
Produkt(7bR,11aS)-N-(2,3-dichlorophenyl)-1,2,7b,8,9,10,11,11 a-octahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indol-6-amineHCID 60071808—

Reaktionsschritte

Using 1-bromo-2,3-dichlorobenzene and following the procedures described in EXAMPLE 33, Parts C and D, tert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-pyrido[4,3-b][1,4]thiazepino[6,5,4-hi]indole-9(8H)Carboxylate from EXAMPLE 33, Part B was converted into the title compound of EXAMPLE 37 as a powder. 1H NMR (CDCl3,300 MHz) δ 1.79-1.89 (m, 2H), 2.58-2.69 (m, 1H), 2.79-3.25 (m, 7H), 3.41-3.50 (m, 1H), 3.60-3.68 (m, 2H), 3.74 (s, 2H), 6.01 (s, 1H), 6.73 (d, 1H, J=2 Hz), 6.81-6.85 (m, 3H), 6.95-6.98 (m 1H). LRMS (ES)+: 406 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849619B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-22d98f363aa94914b31e4939e9d8c9e8
Quellennotizuspto-grants-2005_02