홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Bicarbonate → N2-(1-Phenylethyl)-1,3-benzothiazole-2,7-diamine

HRID 2235492
노트
인쇄 미리보기

반응식

HRID 2235492 반응식
[N+:1]([C:4]1[C:12]2[S:11][C:10]([NH:13][CH:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH3:15])=[N:9][C:8]=2[CH:7]=[CH:6][CH:5]=1)([O-])=O.C(=O)(O)[O-].[Na+]>CN(C=O)C>[C:16]1([CH:14]([NH:13][C:10]2[S:11][C:12]3[C:4]([NH2:1])=[CH:5][CH:6]=[CH:7][C:8]=3[N:9]=2)[CH3:15])[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516892Sodium BicarbonateHCID 588965417-nitro-N-(1-phenylethyl)-1,3-benzothiazol-2-amine

생성물 1

HCID 58896511N2-(1-Phenylethyl)-1,3-benzothiazole-2,7-diamine수율 11%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To 0.165 g (0.55 mmol) of 7-nitro-N-(1-phenylethyl)-1,3-benzothiazol-2-amine in 10 mL of DMF was added 0.62 g (2.8 mmol) of stannous chloride dihydrate. The reaction was heated to 80° C. for 48 h and neutralized with saturated sodium bicarbonate. The mixture was filtered through celite and extracted with ethyl acetate. The extracts were dried in vacuo and purified by flash chromatography eluting with a 50-75% ethyl acetate/hexanes gradient mixture to give 0.016 g (11%) of the title compound as a light yellow solid.

후처리

  1. filtrationThe mixture was filtered through celite
  2. extractionextracted with ethyl acetate
  3. customThe extracts were dried in vacuo
  4. custompurified by flash chromatography
  5. washeluting with a 50-75% ethyl acetate/hexanes gradient mixture

출처 및 근거

ORD 기록
ord-d81079efaad04469a23f0ff0df11231f
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714009B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트