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6-Chloro[1,3]dioxolo[4,5-f][1,3]benzothiazole → HCID 178527754, 화합물

HRID 2399724
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HRID 2399724 반응식
Cl[C:2]1[S:3][C:4]2[CH:10]=[C:9]3[O:11][CH2:12][O:13][C:8]3=[CH:7][C:5]=2[N:6]=1.NC(N)=[S:16]>C(O)C>[SH:16][C:2]1[S:3][C:4]2[CH:10]=[C:9]3[O:11][CH2:12][O:13][C:8]3=[CH:7][C:5]=2[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 20498846-Chloro[1,3]dioxolo[4,5-f][1,3]benzothiazoleHCID 2723790Thiourea

생성물 1

HCID 178527754HCID 178527754, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

The product from Step 2 (0.67 g) and thiourea (0.26 g) were mixed in ethanol (20 cm3) and stirred and heated to reflux under an atmosphere of nitrogen for 18 hr. The pale yellow solid which precipitated was filtered from the solution at ambient temperature, washed with ethanol and sucked to dryness to give the required product. 1H NMR (DMSO): δ7.26(1H,s); 6.80(1H,s); 6.02(2H,s); mp 265° C. (dec); M+ =211.

후처리

  1. temperatureheated
  2. temperatureto reflux under an atmosphere of nitrogen for 18 hr
  3. customThe pale yellow solid which precipitated
  4. filtrationwas filtered from the solution at ambient temperature
  5. washwashed with ethanol

출처 및 근거

ORD 기록
ord-0d8b9693e20043679f50682ffbbf8374
출처 데이터셋
uspto-grants-1995_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05451594

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