5-amino-7-chloro-3-(2-fluorobenzyl)-3H-1,2,3-triazolo[4,5-d]pyrimidine → HCID 178508329, 화합물

HRID 723433

반응식

HRID 723433 반응식
Cl[C:2]1[C:3]2[N:11]=[N:10][N:9](CC3C=CC=CC=3F)[C:4]=2[N:5]=[C:6]([NH2:8])[N:7]=1.C([Sn](CCCC)(CCCC)C1N(COCC[Si](C)(C)C)N=NC=1)CCC>CN(C=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[N:11]1[C:3]2[CH:2]=[N:7][C:6]([NH2:8])=[N:5][C:4]=2[NH:9][N:10]=1

참가 물질

5

반응물 2

HCID 218745675-amino-7-chloro-3-(2-fluorobenzyl)-3H-1,2,3-triazolo[4,5-d]pyrimidineHCID 68893656tributyl 1-(2-(trimethylsilyl)ethoxymethyl)-1H-triazol-5-ylstannane

생성물 1

HCID 178508329HCID 178508329, 화합물

시약·촉매·용매 2

HCID 178418476HCID 178418476, 화합물촉매HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

A mixture of 7-chloro-3-(2-fluorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine (145 mg, 0.50 mmol), tributyl 1-(2-(trimethylsilyl)ethoxymethyl)-1H-triazol-5-ylstannane (336 mg, 0.75 mmol) and Pd(PPh3)2Cl2 (35 mg, 0.05 mmol) in DMF (2 mL) was shaken at 80° C. for 17 h then purified directly by chromatography [SiO2; iso-hexane:EtOAc (2:1)] to give 3-(2-fluorobenzyl)-7-(1-(2-trimethylsilyl)ethoxymethyl)-1H-triazol-5-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine as a colourless oil. This material was dissolved in MeOH (1 mL), treated with a solution of HCl (0.5 mL, 4-M in dioxane), stirred for 17 h, concentrated in vacuo and the residue triturated with Et2O to give the title compound (16 mg, 10%) as an off-white solid.

후처리

  1. customthen purified directly by chromatography [SiO2; iso-hexane:EtOAc (2:1)]

출처 및 근거

ORD 기록
ord-ac50835f8cab496b9f0fbd32cb1f8006
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07141575B2

연결된 노트

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