C₁₈H₂₁N₅O₃S

Base Information

Chemical Name:C₁₈H₂₁N₅O₃S
CAS No.:1422360-67-5
Molecular Formula:C₁₈H₂₁N₅O₃S
Molecular Weight:387.462
Hs Code.:

C<sub>18</sub>H<sub>21</sub>N<sub>5</sub>O<sub>3</sub>S

Synonyms:

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Chemical Property of C₁₈H₂₁N₅O₃S

Chemical Property:

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Technology Process of C₁₈H₂₁N₅O₃S

There total 10 articles about C₁₈H₂₁N₅O₃S 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:

: C₂₄H₃₅N₅O₃SSi

: 1422360-67-5
C₁₈H₂₁N₅O₃S

Guidance literature:: With hydrogenchloride; In methanol; water; at 20 ℃; for 0.0833333h; Inert atmosphere;
DOI:10.1021/jm301499r

Reference yield:

: C₁₈H₂₆N₂O₅

: 1422360-67-5
C₁₈H₂₁N₅O₃S

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid / methanol / 49.5 h / 20 - 67 °C / Inert atmosphere

2: tert.-butylnitrite; copper dichloride / dichloromethane; acetonitrile / 1.5 h / 65 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / acetonitrile / 80 °C / Inert atmosphere

4: hydrogenchloride / methanol; water / 0.08 h / 20 °C / Inert atmosphere

With hydrogenchloride; tert.-butylnitrite; acetic acid; N-ethyl-N,N-diisopropylamine; copper dichloride; In methanol; dichloromethane; water; acetonitrile; 2: |Sandmeyer Reaction;
DOI:10.1021/jm301499r

Reference yield:

: 2040-04-2
2,6-dimethoxyacetophenone

: 1422360-67-5
C₁₈H₂₁N₅O₃S

Guidance literature:: Multi-step reaction with 6 steps

1: phenyltrimethylammonium tribromide / tetrahydrofuran / Inert atmosphere

2: tetrahydrofuran / 48 h / 67 °C / Inert atmosphere

3: acetic acid / methanol / 49.5 h / 20 - 67 °C / Inert atmosphere

4: tert.-butylnitrite; copper dichloride / dichloromethane; acetonitrile / 1.5 h / 65 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine / acetonitrile / 80 °C / Inert atmosphere

6: hydrogenchloride / methanol; water / 0.08 h / 20 °C / Inert atmosphere

With hydrogenchloride; tert.-butylnitrite; phenyltrimethylammonium tribromide; acetic acid; N-ethyl-N,N-diisopropylamine; copper dichloride; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile; 4: |Sandmeyer Reaction;
DOI:10.1021/jm301499r