N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

Base Information

Chemical Name:N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride
CAS No.:1130020-67-5
Molecular Formula:C₂₉H₃₄N₂O₃*ClH
Molecular Weight:495.061
Hs Code.:

Synonyms:N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

Chemical Property:

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Technology Process of N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

There total 5 articles about N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride 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: 59.0%

: 1130021-10-1
N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide

: 1130020-67-5
N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

Guidance literature:: With hydrogenchloride; In methanol;
DOI:10.1016/j.bmc.2010.12.035

Reference yield:

: 1103501-77-4
C₂₂H₂₈N₄O₂

: 1130020-67-5
N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: palladium 10% on activated carbon; camphor-10-sulfonic acid; hydrogen / methanol / 12 h / 20 °C

2: pyridine / 3 h / 20 °C / Inert atmosphere

3: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere

4: 1-thiopropane; potassium tert-butylate / N,N-dimethyl-formamide / 150 °C

5: hydrogenchloride / methanol

With pyridine; hydrogenchloride; 1-thiopropane; palladium 10% on activated carbon; camphor-10-sulfonic acid; potassium tert-butylate; hydrogen; sodium hydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.bmc.2010.12.035

Reference yield:

: 1103501-78-5
(17-cyclopropylmethyl-6β,14β-epoxy-3-methoxymorphinan-6α-yl)methanamine

: 1130020-67-5
N-[(17-cyclopropylmethyl-6β,14β-epoxy-3-hydroxymorphinan-6α-yl)methyl]-N-methylbenzamide hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 3 h / 20 °C / Inert atmosphere

2: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere

3: 1-thiopropane; potassium tert-butylate / N,N-dimethyl-formamide / 150 °C

4: hydrogenchloride / methanol

With pyridine; hydrogenchloride; 1-thiopropane; potassium tert-butylate; sodium hydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.bmc.2010.12.035