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Acetic Acid → [1,3]Thiazolo[4,5-b]pyrazine-2(3H)-thione

HRID 547338
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HRID 547338 반응식
[NH2:1][C:2]1[C:7](Cl)=[N:6][CH:5]=[CH:4][N:3]=1.O(CC)[C:10]([S-:12])=[S:11].[K+].CN1CCCC1=O.C(O)(=O)C>O>[S:12]1[C:7]2[C:2](=[N:3][CH:4]=[CH:5][N:6]=2)[NH:1][C:10]1=[S:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 13387N-methyl-2-pyrrolidoneHCID 2762242-Amino-3-chloropyrazineHCID 2735045Potassium ethylxanthate

생성물 1

HCID 13772324[1,3]Thiazolo[4,5-b]pyrazine-2(3H)-thione수율 67%

시약·촉매·용매 1

HCID 962Water용매

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온도
150 °C

실험 절차

To a mixture of 2-amino-3-chloropyrazine (5.0 g, 38.6 mmol) and potassium ethyl xanthate (9.28 g, 57.9 mmol) was added 1-methyl-2-pyrrolidinone (68 mL). The solution was stirred and heated at 150° C. for 16 h. After cooling to rt, glacial acetic acid (10 mL) and water (1500 mL) were added to the solution. The solid precipitate was filtered. The solid was suspended in 1:1 EtOH/water (500 mL) and sonicated. The solid was once again filtered, washed with water, and dried with CaSO4 in vacuo for 16 h to yield the product (4.36 g, 67%). 1H NMR (500 MHz, DMSO-d6): 14.69 (br s, 1H), 8.42 (d, J=2.8, 1H), 8.39 (d, J=2.8, 1H). MS (ESI): mass calcd. for C5H3N3S2, 168.98; m/z found, 170.00 [M+H]+.

후처리

  1. temperatureAfter cooling to rt
  2. filtrationThe solid precipitate was filtered
  3. customsonicated
  4. filtrationThe solid was once again filtered
  5. washwashed with water
  6. dry with materialdried with CaSO4 in vacuo for 16 h

출처 및 근거

ORD 기록
ord-3f0baaf0146a4650baa2d9e914070415
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939527B2

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