tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

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Chemical Name:tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate
CAS No.:1383715-58-9
Molecular Formula:C₂₁H₂₃ClF₂N₄O₄S
Molecular Weight:500.954
Hs Code.:

Synonyms:tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

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Chemical Property of tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

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Technology Process of tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

There total 9 articles about tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 145783-14-8
4,6-dichloro-5-nitro-2-(propylsulfanyl)pyrimidine

: 1350749-64-2
tert-butyl ((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

: 1383715-58-9
tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at -80 - -75 ℃; for 2h; Time; Inert atmosphere;

Reference yield:

: 1006614-49-8,220352-38-5,1459719-81-3
(1R,2S)-2-(3,4-difluorophenyl)cyclopropanamine

: 1383715-58-9
tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: methanol / 12 h / 20 - 25 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 20 - 25 °C

2.2: 3 h / 20 - 25 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -25 - -15 °C

3.2: 1.5 h / -25 - -15 °C

3.3: 0.08 h

With N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1383715-58-9
tert-butyl (6-chloro-5-nitro-2-(propylthio)pyrimidin-4-yl)((1R,2S)-2-(3,4-difluorophenyl)cyclopropyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 1 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 16 h / 20 °C

With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil;