Methyl iodide → (4bS,8R,8aS,9aR,10S,13aR,13bR)-10-tert-butyl-7-cyclopropylmethyl-5,6,7,8,9,9a,10,13b-octahydro-1-methoxy-10-methyl-8a,13a-ethano-4,8-methanobenzofuro[3,2-e][1,3]dioxino[4,5-g]isoquinoline

HRID 629833Notes

Reaction equation

[CH2:1]([O:8][C:9]1[C:14]2[O:15][C@H:16]3[C@@:25]45[CH2:35][CH2:36][C@:22]6([CH2:23][C@@H:24]4[C@:29]([C:31]([CH3:34])([CH3:33])[CH3:32])([CH3:30])[O:28][CH2:27][O:26]5)[C@@:17]43[CH2:18][CH2:19][N:20]([CH2:38][CH:39]3[CH2:41][CH2:40]3)[C@@H:21]6[CH2:37][C:12]([C:13]=24)=[CH:11][CH:10]=1)C1C=CC=CC=1.CI>>[C:31]([C@:29]1([CH3:30])[C@@H:24]2[C@@:25]3([CH2:35][CH2:36][C@:22]4([CH2:23]2)[C@@:17]25[C:13]6[C:12](=[CH:11][CH:10]=[C:9]([O:8][CH3:1])[C:14]=6[O:15][C@@H:16]32)[CH2:37][C@H:21]4[N:20]([CH2:38][CH:39]2[CH2:40][CH2:41]2)[CH2:19][CH2:18]5)[O:26][CH2:27][O:28]1)([CH3:34])([CH3:32])[CH3:33]

Participants

Reactant 2

HCID 6328Methyl iodide

HCID 121278739(4bS,8R,8aS,9aR,10S,13aR,13bR)-1-benzyloxy-10-tert-butyl-7-cyclopropylmethyl-5,6,7,8,9,9a,10,13b-octahydro-10-methyl-8a,13a-ethano-4,8-methanobenzofuro[3,2-e][1,3]dioxino[4,5-g]isoquinoline

Product 1

HCID 89985177(4bS,8R,8aS,9aR,10S,13aR,13bR)-10-tert-butyl-7-cyclopropylmethyl-5,6,7,8,9,9a,10,13b-octahydro-1-methoxy-10-methyl-8a,13a-ethano-4,8-methanobenzofuro[3,2-e][1,3]dioxino[4,5-g]isoquinolineYield 49.4%

Procedure

The title compound 8 was synthesized similar to the procedure described in Example 5 for compound 7 using methyl iodide instead of benzyl bromide. After column chromatography, 418 mg (49.4% yield) of compound 8 was isolated in a purity of 98.8% as an white solid.

Workup

customThe title compound 8 was synthesized similar to the procedure

Sources & evidence

ORD record: ord-abb6d45318e74e019807ba4c8aea29fb
Source dataset: uspto-grants-2016_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09315514B2

Reaction notes

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