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Triethylamine → HCID 69245143, compound

HRID 2113548
Notes
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Reaction equation

HRID 2113548 reaction equation
Cl[C:2]1[O:3][C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:5][N:6]=1.[F:13][C:14]([F:33])([F:32])[C:15]1[CH:16]=[C:17]([N:21]2[CH2:26][CH2:25][N:24]([CH2:27][CH2:28][CH2:29][CH2:30]N)[CH2:23][CH2:22]2)[CH:18]=[CH:19][CH:20]=1.C([N:36](CC)CC)C>O1CCCC1>[F:33][C:14]([F:13])([F:32])[C:15]1[CH:16]=[C:17]([N:21]2[CH2:22][CH2:23][N:24]([CH2:27][CH2:28][CH2:29][CH2:30][C:2]3[O:3][C:4]([C:7]4[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=4)=[C:5]([NH2:36])[N:6]=3)[CH2:25][CH2:26]2)[CH:18]=[CH:19][CH:20]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 109976262-Chloro-5-phenyloxazoleHCID 111624114-(4-(3-(Trifluoromethyl)phenyl)piperazin-1-yl)butan-1-amine

Product 1

HCID 69245143HCID 69245143, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

A solution of 35 mg (0.2 mmol) of 2-chloro-5-phenyloxazole in 0.5 mL of tetrahydrofuran is added, at 0° C., to a solution of 62 mg (0.2 mmol) of 4-[4-(3-trifluoromethylphenyl)piperazine-1-yl]butylamine (Example 3, step b) and 20 mg (0.2 mmol) of triethylamine in 0.2 mL of tetrahydrofuran. The mixture is stirred overnight under argon.

Sources & evidence

ORD record
ord-27bc0977600f44269f43b8ba09e81b56
Source dataset
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07432269B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes