HCID 18008045, compound → HCID 18008093, compound

HRID 2117219Notes

Reaction equation

HRID 2117219 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][CH2:13][CH2:14][OH:15].Br[CH2:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:19]=1[O:20][CH2:21][C:22]#[N:23]>>[CH3:17][C:18]1[CH:27]=[CH:26][CH:25]=[C:24]([CH2:28][O:15][CH2:14][CH2:13][O:12][CH2:11][C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[N:1]=2)[C:19]=1[O:20][CH2:21][C:22]#[N:23]

Participants

3

Reactant 2

HCID 18008045HCID 18008045, compoundHCID 222414892-Cyanomethoxy-3-methylbenzyl bromide

Product 1

HCID 18008093HCID 18008093, compound

Procedure

MS (ESI) 363 (M+H)+. Prepared from 2-(quinolin-2-ylmethoxy)-ethanol (EXAMPLE 34d) and (2-bromomethyl-6-methyl-phenoxy)-acetonitrile.

Sources & evidence

ORD record
ord-5858d4b0a8294d93ac073900e669ad39
Source dataset
uspto-grants-2008_10
Patent number
USRE040558E1

Reaction notes

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