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Azido(trimethyl)stannane → HCID 178507543, 화합물

HRID 1711312
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HRID 1711312 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]#[N:10])=[CH:4][C:3]=1[C:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH:12]=1.[N:17]([Sn](C)(C)C)=[N+:18]=[N-:19]>C1(C)C=CC=CC=1>[C:11]1([C:3]2[CH:4]=[C:5]([CH2:8][C:9]3[NH:19][N:18]=[N:17][N:10]=3)[CH:6]=[CH:7][C:2]=2[NH2:1])[CH2:16][CH2:15][CH2:14][CH2:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5104973Azido(trimethyl)stannaneHCID 58754819(4-Amino-3-cyclohex-1-enyl-phenyl)-acetonitrile

생성물 1

HCID 178507543HCID 178507543, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

The title compound was prepared from (4-amino-3-cyclohex-1-enyl-phenyl)-acetonitrile (as prepared in the previous step, 103 mg, 0.485 mmol) and azidotrimethylstannane (105 mg, 0.510 mmol) in toluene (4 mL) according to the procedure in Example 52, step (c) and then further purified by preparative TLC (10% MeOH—CHCl3) to afford 40 mg (39%) as a white solid. Mass spectrum (ESI, m/z): Calcd. for C14H17N5, 256.1 (M+H), found 256.1.

후처리

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  1. customfurther purified by preparative TLC (10% MeOH—CHCl3)
  2. customto afford 40 mg (39%) as a white solid

출처 및 근거

ORD 기록
ord-f401da7a451c4d3a96efe5d310a48400
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07790724B2

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