1-Ethynyl-4-fluorobenzene → 3,4-bis(Benzyloxy)-6-[(4-fluorophenyl)ethynyl]pyridazine

HRID 927059Notes

Reaction equation

HRID 927059 reaction equation
[CH2:1]([O:8][C:9]1[N:10]=[N:11][C:12]([C:23]#[C:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:13][C:14]=1[O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC1N=NC(Cl)=CC=1OCC1C=CC=CC=1)C1C=CC=CC=1.C(C1C=CC([F:62])=CC=1)#C>>[CH2:1]([O:8][C:9]1[N:10]=[N:11][C:12]([C:23]#[C:24][C:25]2[CH:30]=[CH:29][C:28]([F:62])=[CH:27][CH:26]=2)=[CH:13][C:14]=1[O:15][CH2:16][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 5226271-Ethynyl-4-fluorobenzeneHCID 122134743,4-Bis(benzyloxy)-6-chloropyridazine2×HCID 712704193,4-Bis(benzyloxy)-6-(phenylethynyl)pyridazine2×

Product 1

HCID 712702413,4-bis(Benzyloxy)-6-[(4-fluorophenyl)ethynyl]pyridazineYield 72%

Procedure

Prepared as described for 3,4-bis(benzyloxy)-6-(phenylethynyl)pyridazine (Intermediate 2) from 3,4-bis(benzyloxy)-6-chloropyridazine (Intermediate 1) and 1-ethynyl-4-fluorobenzene in 72% yield.

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-c867f7a1e1f94503b6e8d04243a0795d
Source dataset
uspto-grants-2016_03
Patent number
US09290456B2

Reaction notes

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