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1,1,1-trimethyl-N-((trimethylsilyl)oxy)silylamine → N*5*-(3,5-Dichloro-phenyl)-[1,2,4]oxadiazole-3,5-diamine

HRID 1048862
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HRID 1048862 반응식
[C:1](/[N:3]=[C:4](\SC)/[NH:5][C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[C:8]([Cl:13])[CH:7]=1)#[N:2].C[Si](C)(C)[NH:18][O:19][Si](C)(C)C>C(Cl)(Cl)(Cl)Cl>[Cl:12][C:10]1[CH:11]=[C:6]([NH:5][C:4]2[O:19][N:18]=[C:1]([NH2:2])[N:3]=2)[CH:7]=[C:8]([Cl:13])[CH:9]=1
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참가 물질

4

반응물 2

HCID 898151,1,1-trimethyl-N-((trimethylsilyl)oxy)silylamineHCID 178503892HCID 178503892, 화합물

생성물 1

HCID 85469493N*5*-(3,5-Dichloro-phenyl)-[1,2,4]oxadiazole-3,5-diamine수율 22%

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

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온도
80 °C

실험 절차

In a 5 mL microwave vial, (Z)-methyl N′-cyano-N-(3,5-dichlorophenyl)carbamimidothioate (156 mg, 0.6 mmol, Eq: 1.00) and N,O-bis(trimethylsilyl)hydroxylamine (160 mg, 900 μmol, Eq: 1.5) were combined with CCl4 (1 ml) to give a colorless suspension which was capped and heated in a 80° C. oil bath for 2.5 hr. The mixture was concentrated in vacuo and MeOH added. The mixture was stirred at RT for 18 hours. The reaction mixture was concentrated in vacuo and the crude material was purified by preparative TLC (silica gel, 1.0 mm, 9:1 DCM/MeOH) to give product which was recrystallized from MeOH and dried in vacuo (89° C., 2 torr, overnight) to give 32 mg (22%) of desired product as a light brown solid.

후처리

  1. customto give a colorless suspension which
  2. customwas capped
  3. concentrationThe mixture was concentrated in vacuo and MeOH
  4. additionadded
  5. concentrationThe reaction mixture was concentrated in vacuo
  6. customthe crude material was purified by preparative TLC (silica gel, 1.0 mm, 9:1 DCM/MeOH)
  7. customto give product which
  8. customwas recrystallized from MeOH
  9. customdried in vacuo (89° C., 2 torr, overnight)

출처 및 근거

ORD 기록
ord-f56b8cd1cb0c4c449ffb382609d13e6d
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382218B2

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