864377-31-1

Basic information

• Product Name: 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine
• Synonyms: 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine;1,3,5-Triazine, 2-(3-bromophenyl)-4,6-diphenyl-
• CAS NO: 864377-31-1
• Molecular Formula: C₂₁H₁₄BrN₃
• Molecular Weight: 388.25996
• Product Categories: 1,3,5-triazine
• Mol File: 864377-31-1.mol
• Article Data: 41

Chemical Properties

• Melting Point: 174.0 to 178.0 °C
• Boiling Point: 573.9 °C at 760 mmHg
• Flash Point: 300.9 °C
• Appearance: /
• Density: 1.381
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 0.65±0.10(Predicted)
• CAS DataBase Reference: 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine(864377-31-1)
• EPA Substance Registry System: 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine(864377-31-1)

Safety Data

• Hazardous Substances Data: 864377-31-1(Hazardous Substances Data)

Usage

Uses

2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine is a useful research chemical.

Chemical Properties

white powder

Synthetic route

2-chloro-4,6-diphenyl-1,3,5-triazine (3842-55-5) + (3-bromophenyl)boronic acid (89598-96-9) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%

(3-Bromophenyl)methanol (15852-73-0) + benzamidin (618-39-3) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With oxygen In toluene at 110℃; for 20h; Schlenk technique;	90%

benzamidine monohydrochloride (1670-14-0) + 3-bromobenzyl chloride (932-77-4) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With sodium carbonate; sulfur In dimethyl sulfoxide at 130℃; for 24h;	90%
With sulfur; potassium hydroxide In dimethyl sulfoxide at 130℃; for 24h; Sealed tube;	88%

2-bromo-4,6-diphenyl-1,3,5-triazabenzene (80984-79-8) + (3-bromophenyl)boronic acid (89598-96-9) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 90℃; for 5h; Inert atmosphere;	87.46%
Suzuki Coupling;
Suzuki Coupling;

1-Bromo-3-iodobenzene (591-18-4) + ((4,6-diphenyl-1,3,5-triazin-2-yl)boronic acid) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 90℃; for 5h; Inert atmosphere;	83.1%

1-Bromo-3-iodobenzene (591-18-4) + 2,4-diphenyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-1,3,5-triazine → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water for 10h; Suzuki Coupling; Inert atmosphere; Reflux;	83%

m-bromobenzoic aldehyde (3132-99-8) + benzamidine monohydrochloride (1670-14-0) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With nickel diacetate; sodium carbonate In toluene at 110℃; for 30h; Reagent/catalyst;	83%
With copper(II) acetate monohydrate; sodium carbonate In toluene at 100℃; for 24h;	68%
With sodium carbonate; copper(l) chloride at 90 - 100℃;	3.2 g

N-(3-bromobenzylidene)-phenyl-amine (18467-14-6) + benzamidine monohydrochloride (1670-14-0) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With sodium hydroxide In ethanol for 12h; Reflux;	74%
Stage #1: N-(3-bromobenzylidene)-phenyl-amine; benzamidine monohydrochloride With sodium hydroxide In ethanol at 80℃; for 16h; Inert atmosphere; Stage #2: With sodium t-butanolate In ethanol at 80℃; for 16h; Inert atmosphere;	37%
Stage #1: N-(3-bromobenzylidene)-phenyl-amine; benzamidine monohydrochloride With sodium hydroxide In ethanol at 80℃; for 16h; Inert atmosphere; Stage #2: With sodium t-butanolate In ethanol at 80℃; for 16h;	37%
Stage #1: N-(3-bromobenzylidene)-phenyl-amine; benzamidine monohydrochloride With sodium hydroxide In ethanol for 18h; Inert atmosphere; Reflux; Stage #2: With sodium t-butanolate In ethanol for 16h; Inert atmosphere; Reflux;	26.7%

3-bromobenzoyl chloride (1711-09-7) + benzamidine monohydrochloride (1670-14-0) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Stage #1: 3-bromobenzoyl chloride; benzamidine monohydrochloride With triethylamine In 5,5-dimethyl-1,3-cyclohexadiene at 0 - 60℃; for 3.5h; Inert atmosphere; Stage #2: With 1,1,3,3-tetramethyldisilazane In 5,5-dimethyl-1,3-cyclohexadiene at 150℃; for 5h; Inert atmosphere;	72%

2-chloro-4,6-diphenyl-1,3,5-triazine (3842-55-5) + (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)bromobenzene) (594823-67-3) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane for 5h; Inert atmosphere; Reflux;	72%

3-bromobenzoyl chloride (1711-09-7) + benzonitrile (100-47-0) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Stage #1: 3-bromobenzoyl chloride; benzonitrile In dichloromethane at 0 - 5℃; for 0.5h; Inert atmosphere; Cooling with ice; Stage #2: With antimonypentachloride In dichloromethane at 20℃; for 1h; Inert atmosphere; Stage #3: With ammonia In water at 0 - 20℃; for 3.5h; Cooling with ice;	66.7%
Stage #1: 3-bromobenzoyl chloride; benzonitrile With aluminum (III) chloride; thionyl chloride In 1,2-dichloro-benzene at 100℃; for 20h; Stage #2: With ammonium chloride In 1,2-dichloro-benzene at 100℃; for 3h;	40%

m-bromobenzoic aldehyde (3132-99-8) + benzimidamide hydrochloride → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
With sodium carbonate; copper dichloride In toluene at 130℃;	52%

1,3-dibromobenzene (108-36-1) + 2-chloro-4,6-diphenyl-1,3,5-triazine (3842-55-5) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Stage #1: 1,3-dibromobenzene With n-butyllithium In tetrahydrofuran-d8 at -78℃; for 1h; Stage #2: 2-chloro-4,6-diphenyl-1,3,5-triazine In tetrahydrofuran at 20℃; for 5h;	40.4%
With n-butyllithium In tetrahydrofuran at -78 - 20℃; for 12h;	28%
Stage #1: 1,3-dibromobenzene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Stage #2: 2-chloro-4,6-diphenyl-1,3,5-triazine In tetrahydrofuran; hexane at 20℃; for 3h;

1-Bromo-3-iodobenzene (591-18-4) + 2-chloro-4,6-diphenyl-1,3,5-triazine (3842-55-5) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Stage #1: 1-Bromo-3-iodobenzene With n-butyllithium In tetrahydrofuran at -78℃; for 1.5h; Inert atmosphere; Stage #2: 2-chloro-4,6-diphenyl-1,3,5-triazine In tetrahydrofuran at 20℃; for 1.5h; Inert atmosphere;	30%
With n-butyllithium In tetrahydrofuran at -78℃; for 2h; Inert atmosphere;	30%
Stage #1: 1-Bromo-3-iodobenzene With n-butyllithium In tetrahydrofuran at -78℃; for 1.5h; Inert atmosphere; Stage #2: 2-chloro-4,6-diphenyl-1,3,5-triazine In tetrahydrofuran at -78 - 20℃; for 1.5h; Inert atmosphere;	30%

m-bromobenzoic aldehyde (3132-99-8) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Multi-step reaction with 2 steps 1.1: toluene / 8 h / Reflux 2.1: sodium hydroxide / ethanol / 16 h / 80 °C / Inert atmosphere 2.2: 16 h / 80 °C / Inert atmosphere View Scheme
Multi-step reaction with 2 steps 1: ethanol / 3 h / 20 °C 2: sodium hydroxide / ethanol / 12 h / Reflux View Scheme
Multi-step reaction with 2 steps 1.1: toluene / 8 h / Reflux 2.1: sodium hydroxide / ethanol / 16 h / 80 °C / Inert atmosphere 2.2: 16 h / 80 °C View Scheme
Multi-step reaction with 2 steps 1.1: toluene / 8 h / Inert atmosphere; Reflux; Dean-Stark 2.1: sodium hydroxide / ethanol / 18 h / Inert atmosphere; Reflux 2.2: 16 h / Inert atmosphere; Reflux View Scheme

2-chloro-4,6-diphenyl-1,3,5-triazine (3842-55-5) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Multi-step reaction with 2 steps 1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; tricyclohexylphosphine / N,N-dimethyl-formamide / 12 h / Inert atmosphere; Reflux 2: tetrakis(triphenylphosphine) palladium(0); potassium carbonate / tetrahydrofuran; water / 10 h / Inert atmosphere; Reflux View Scheme

phenylboronic acid (98-80-6) → 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1)

Conditions	Yield
Multi-step reaction with 2 steps 1: potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; toluene; water / 6 h / 100 °C 2: potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; toluene / 12 h / 100 °C View Scheme

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + bis(pinacol)diborane (73183-34-3) → 4,4,5,5-tetramethyl-2-(5'-phenyl-[1,1’:3' ,1"-terphenyl]-4-yl)-1,3,2-dioxaborolane

Conditions	Yield
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In 1,4-dioxane for 17h; Reflux;	96%
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate In 1,4-dioxane at 90℃; for 12h; Reflux;	96.8%
With bis-triphenylphosphine-palladium(II) chloride; potassium acetate In tetrahydrofuran at 80℃; for 3h; Inert atmosphere;	93%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 3-(2-pyridyl)-9H-carbazole → 3-(3-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-9H-carbazole

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,4-dioxane; water for 17h; Inert atmosphere; Reflux;	96%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 2-(2,8-diphenyldibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → C45H29N3S

Conditions	Yield
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0) In 1,2-dimethoxyethane; water; toluene for 16h; Inert atmosphere; Reflux;	95%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 3-chlorophenylboronic acid (63503-60-6) → 2-(3'-chloro-[1,1'-biphenyl]-3-yl)-4,6-diphenyl-1,3,5-triazine

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water at 80℃; for 12h; Inert atmosphere;	95%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C24H15N → C45H28N4

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene at 110℃; for 15h; Inert atmosphere;	95%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C24H13NO → C45H26N4O

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene for 3h; Reflux;	95%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C28H18Br2Cl2SiZn2 → C70H46Br2N6Si

Conditions	Yield
In toluene for 12h; Inert atmosphere; Reflux;	94%

((3-(dibenzo[b,d]thiophen-4-yl)phenyl)boronic acid) (1307859-67-1) + 2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) → 2-(3'-(dibenzo[b,d]thiophen-4-yl)-[1,1'-biphenyl]-3-yl)-4,6-diphenyl-1,3,5-triazine

Conditions	Yield
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0) In tetrahydrofuran; water for 1h; Suzuki-Miyaura Coupling; Reflux; Inert atmosphere;	93%
With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0) In tetrahydrofuran; water at 80℃; for 15h; Inert atmosphere;	81.5%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 2-phenyl-4H-thieno[3,2-b]indole → C37H24N4S

Conditions	Yield
With tri-tert-butyl phosphine; sodium t-butanolate In toluene for 12h; Reflux; Inert atmosphere;	92%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,10-phenanthroline → 4,6-diphenyl-2-[3-(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine

Conditions	Yield
With palladium diacetate; caesium carbonate; triphenylphosphine In tetrahydrofuran for 19h; Inert atmosphere; Reflux;	91%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C27H19NO → C48H32N4O

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium t-butanolate In 5,5-dimethyl-1,3-cyclohexadiene at 145℃; for 3h; Inert atmosphere;	90%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 7H-spiro[chromeno[2,3-b]carbazole-13,9'-fluorene] → C52H32N4O

Conditions	Yield
With bis(tri-t-butylphosphine)palladium(0); sodium t-butanolate In 5,5-dimethyl-1,3-cyclohexadiene for 4h; Inert atmosphere; Reflux;	90%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + anthracene-9-boronic acid (100622-34-2) → 2-(3-(anthracen-9-yl)phenyl)-4,6-diphenyl-1,3,5-triazine

Conditions	Yield
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In ethanol; water; toluene for 22h; Inert atmosphere; Reflux;	90%
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate In ethanol; water; toluene for 18h; Inert atmosphere; Reflux;	90%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + (5-phenyl-5H-benzofuro[3,2-c]carbazol-11-yl)boronic acid → C45H28N4O

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In tetrahydrofuran; water for 12h; Reflux; Inert atmosphere;	90%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 2-(5-(dibenzo[b,d]thiophen-4-yl)-[1,1'-biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → C45H29N3S

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In 1,2-dimethoxyethane; water for 14h; Inert atmosphere; Reflux;	89%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C22H13NO2 → C43H26N4O2

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene for 5h; Inert atmosphere; Reflux;	89%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C12H7N3S → C33H20N6S

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate In toluene for 5h; Inert atmosphere; Reflux;	89%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C22H15N → C43H28N4

Conditions	Yield
Stage #1: 2-(3-bromophenyl)-4,6-diphenyl-[1,3,5]triazine; C22H15N With sodium t-butanolate In 5,5-dimethyl-1,3-cyclohexadiene for 0.5h; Heating; Stage #2: With bis(tri-t-butylphosphine)palladium(0) In 1-methyl-pyrrolidin-2-one; 5,5-dimethyl-1,3-cyclohexadiene for 2h; Buchwald-Hartwig Coupling; Reflux;	88.4%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 3-[4-(2-pyridyl)phenyl]carbazole → 3-[4-(2-pyridyl)phenyl]-9-[3-(4,6-diphenyltriazin-2-yl)phenyl]carbazole

Conditions	Yield
With 18-crown-6 ether; tri-tert-butyl phosphine; palladium diacetate; potassium carbonate In 5,5-dimethyl-1,3-cyclohexadiene; toluene for 4h; Inert atmosphere; Reflux;	88%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C26H17BO2 → C47H29N3

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In ethanol; water; toluene for 12h; Inert atmosphere; Reflux;	88%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + B-[6-(9-phenyl-9H-carbazol-3-yl)-4-dibenzofuranyl]boronic acid → 3-{6-[3-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl]dibenzofuran-4-yl}-9-phenyl-9H-carbazole

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In ethanol; water for 16h; Suzuki Coupling; Reflux;	87%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + 4,4,5,5-tetramethyl-2-(7-phenyldibenzo[b,e][1,4]dioxin-2-yl)-1,3,2-dioxaborolane → 2,4-diphenyl-6-(3-(7-phenyldibenzo[b,e][1,4]dioxin-2-yl)phenyl)-1,3,5-triazine

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In water; toluene for 8h; Heating;	87%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C30H17NS → C51H30N4S

Conditions	Yield
With bis(tri-t-butylphosphine)palladium(0); sodium t-butanolate In 5,5-dimethyl-1,3-cyclohexadiene for 11h; Inert atmosphere; Reflux;	87%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C36H25BN2O2 → C57H37N5

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In 1,2-dimethoxyethane; water at 95℃; for 6h; Inert atmosphere;	87%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) → 2-(3-iodophenyl)-4,6-diphenyl-1,3,5-triazine

Conditions	Yield
Stage #1: 2-(3-bromophenyl)-4,6-diphenyl-[1,3,5]triazine With n-butyllithium In tetrahydrofuran at -78℃; for 1h; Inert atmosphere; Stage #2: With iodine In tetrahydrofuran at -78 - 20℃; for 1h; Inert atmosphere;	87%

2-(3-bromo-phenyl)-4,6-diphenyl-1,3,5-triazine (864377-31-1) + C23H14BNO3 → C44H26N4O

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene at 110℃; for 5h; Inert atmosphere;	86.49%

Upstream product

• 864377-28-6 4-(3-Bromophenyl)-2,6-diphenylpyrimidine 
• 864377-22-0 2-(3-bromophenyl)-4,6-diphenylpyrimidine 
• 864376-72-7 Isovaline, N-benzoyl-3,3-dimethyl- (9CI) 
• 864376-61-4 5(4H)-Oxazolone, 4-(1,1-dimethylethyl)-4-methyl-2-phenyl- 
• 864376-58-9 5(4H)-Oxazolone, 4-methyl-4-(1-methylethyl)-2-(4-nitrophenyl)- 
• 864376-57-8 5(4H)-Oxazolone, 4-methyl-4-(1-methylethyl)-2-(3-nitrophenyl)- 
• 864376-56-7 5(4H)-Oxazolone, 2-(3-chlorophenyl)-4-methyl-4-(1-methylethyl)- 
• 864376-55-6 5(4H)-Oxazolone, 4-methyl-4-(1-methylethyl)-2-(4-methylphenyl)- 
• 864376-54-5 5(4H)-Oxazolone, 2-(4-methoxyphenyl)-4-methyl-4-(1-methylethyl)- 
• 864376-14-7 Thiazole, 2-iodo-4-(trifluoroMethyl)- 
• 864376-04-5 Benzothiazole, 6-ethynyl- (9CI) 
• 86437-47-0 C.I. Direct blue 201 
• 86437-46-9 Chromate(5-), bis2-6-4-chloro-6-4-(4-sulfophenyl)azophenylamino-1,3,5-triazin-2-ylamino-1-hydroxy-3-sulfo-2-naphthalenylazobenzoato(4-)-, pentasodium 
• 864373-47-7 OXETANE-2-CARBOXYLIC ACID 

Downstream Products

• 864377-33-3 3-(9H-Carbazol-9-yl)phenylboronic acid 
• 86438-03-1 butane-1,3-diol: hexanedioic acid 
• 86438-26-8 Chemfil 
• 86438-35-9 Cycloteric MV-SF 
• 86438-36-0 Kayarus Supra Yellow GLS 
• 86438-37-1 Dianix Blue FG-SE 
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• 864384-31-6 3(2H)-Pyridazinone,6-amino-4,5-dihydro-5,5-dimethyl-(9CI) 
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• 86438-78-0 LAURAMIDOPROPYL BETAINE 
• 86438-79-1 Cocamidopropyl betaine 

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