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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764906Generated: October 31, 2026

(2,3-Difluorophenyl)boronic acid → (6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,7,8,9,10,10a-octahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole

https://huagongshe.com/reaction/1764906

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3-Difluorophenyl)boronic acidHCID 2734333—
Reactanttert-butyl(6bR,10aS)-5-bromo-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole-8(7H)-carboxylateHCID 21302667—
ReactantTert-butyl(6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole carboxylateHCID 86759405—
Product(6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,7,8,9,10,10a-octahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indoleHCID 6951506296%
ProductTert-butyl(6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole carboxylateHCID 8675940545%

Reaction Steps

Tert-butyl(6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole carboxylate (50 mg, 45%) was prepared by the method of Example 443 Step A as a yellow oil from tert-butyl(6bR,10aS)-5-bromo-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole-8(7H)-carboxylate (100 mg, 0.25 mmol) and 2,3-difluorophenylboronic acid (80 mg, 0.50 mmol). The title compound (22 mg, 96%) was prepared by the method of Example 443 Step B as a yellow oil from tert-butyl(6bR,10aS)-5-(2,3-difluorophenyl)-1,2,6b,9,10,10a-hexahydropyrido[4,3-b][1,4]thiazino[2,3,4-hi]indole carboxylate (30 mg, 0.067 mmol). 1H NMR (CDCl3, 300 MHz) δ1.91-2.05 (m, 2H), 2.60-2.80 (m, 1H), 2.81-3.02 (m, 2H), 3.03-3.18 (m, 2H), 3.20-3.38 (m, 2H), 3.39-3.63 (m, 4H), 6.97 (dd, J=22.4, 2.2 Hz, 1H), 7.02-7.14 (m, 4H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039679E1
Source datasetuspto-grants-2007_06
ORD IDord-fc072239e9bf4b89b3a93753824e8563
Source noteuspto-grants-2007_06