2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Base Information

Chemical Name:2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one
CAS No.:1334758-82-5
Molecular Formula:C₂₉H₃₈N₂O₂SSi
Molecular Weight:506.784
Hs Code.:

Synonyms:2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

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Chemical Property of 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

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Technology Process of 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

There total 9 articles about 2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one 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: 87.0%

: 609-12-1
ethyl 2-bromoisovalerate

: 1191465-55-0
1-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-yl)thiourea

: 1334758-82-5
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In ethanol; at 150 ℃; for 1h; Microwave irradiation;
DOI:10.1021/ml2001467

Reference yield:

: 1334758-61-0
(1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ol

: 1334758-82-5
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Guidance literature:: Multi-step reaction with 6 steps

1: pyridinium chlorochromate / dichloromethane / 16 h / 0 °C

2: L-Selectride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

3: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 32 h / 20 °C / Inert atmosphere

4: hydrazine / ethanol / 3 h / Reflux; Inert atmosphere

5: chloroform / 20 °C / Inert atmosphere

6: N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 150 °C / Microwave irradiation

With L-Selectride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; pyridinium chlorochromate; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; chloroform; 3: Mitsunobu reaction;
DOI:10.1021/ml2001467

Reference yield:

: 1334758-81-4
(1R,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-one

: 1334758-82-5
2-((1R,2S,4R,5S)-5-(tert-butyldiphenylsilyloxy)bicyclo[2.2.1]heptan-2-ylamino)-5-isopropylthiazol-4(5H)-one

Guidance literature:: Multi-step reaction with 5 steps

1: L-Selectride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 32 h / 20 °C / Inert atmosphere

3: hydrazine / ethanol / 3 h / Reflux; Inert atmosphere

4: chloroform / 20 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / ethanol / 1 h / 150 °C / Microwave irradiation

With L-Selectride; N-ethyl-N,N-diisopropylamine; triphenylphosphine; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; chloroform; 2: Mitsunobu reaction;
DOI:10.1021/ml2001467