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Tert-Butyl nitrite → 7-Bromo-6-fluorobenzothiazole

HRID 389583
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HRID 389583 반응식
N[C:2]1[S:3][C:4]2[C:10]([Br:11])=[C:9]([F:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.N(OC(C)(C)C)=O>C1COCC1>[Br:11][C:10]1[C:4]2[S:3][CH:2]=[N:6][C:5]=2[CH:7]=[CH:8][C:9]=1[F:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10906Tert-Butyl nitriteHCID 227204172-Amino-7-bromo-6-fluorobenzothiazole

생성물 1

HCID 667604487-Bromo-6-fluorobenzothiazole수율 34%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
50 °C

실험 절차

To a solution of impure 2-amino-7-bromo-6-fluorobenzothiazole from Step A in THF (10 mL) was added tert-butyl nitrite (90%, 1.25 mL, 9.46 mmol). The mixture was stirred at 50° C. for 7 h and then purified by ISCO chromatography (0 to 40% EtOAc:heptane) to afford 114 mg (34%) of the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3): δ 7.54 (dd, J=2.4, 8.0 Hz, 1H), 7.62 (dd, J=2.4, 8.0 Hz, 1H), 9.03 (s, 1H); 19F NMR (376 MHz, CDCl3): δ−113.77; MS (ESI): 231.92/233.92 [M+H]+; HPLC tR=1.38 min (TOF: polar—3 min).

후처리

  1. custompurified by ISCO chromatography (0 to 40% EtOAc:heptane)

출처 및 근거

ORD 기록
ord-2b3a2480f3684563a76edd4142990b41
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378104B2

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