HCID 22451503, compound → HCID 22451485, compound

HRID 651563Notes

Reaction equation

HRID 651563 reaction equation
[ClH:1].COC[C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]=1[O:15][CH:16]1[CH2:19][NH:18][CH2:17]1.C1(C(C2C=CC=CC=2)N2C[CH:29]([O:31]C3C4C(=CC=CC=4)C=CC=3COC)C2)C=CC=CC=1>>[ClH:1].[CH3:29][O:31][C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]=1[O:15][CH:16]1[CH2:17][NH:18][CH2:19]1

Participants

3

Reactant 2

HCID 22451503HCID 22451503, compoundHCID 22451513HCID 22451513, compound

Product 1

HCID 22451485HCID 22451485, compound

Procedure

3-[(2-(Methoxymethyl)-1-naphthalenyl)oxy]-azetidine hydrochloride, mp 127° C. starting from 1-(diphenylmethyl)-3-[(2-(methoxymethyl)-1-naphtalenyl)oxy]-azetidine.

Sources & evidence

ORD record
ord-8ea9ffad1ee94bc9bcf752745061e1ab
Source dataset
uspto-grants-2001_08
Patent number
US06281243B1

Reaction notes

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