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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Chlorothiophene → 1-Boc-4-(2-thienyl)piperazine

HRID 302
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인쇄 미리보기

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HRID 302 반응식
CC(C)(C)OC(=O)N1CCNCC1.Clc1cccs1>CCN(CC)CC.CN(C)C=O.[Pd].c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1>CC(C)(C)OC(=O)N1CCN(c2cccs2)CC1
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참가 물질

7

반응물 2

HCID 72992-ChlorothiopheneHCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 673439001-Boc-4-(2-thienyl)piperazine수율 0%

시약·촉매·용매 4

HCID 8471Triethylamine시약HCID 11776Triphenylphosphine촉매HCID 11979704Tetrakis(triphenylphosphine)palladium촉매

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온도
95 °C

실험 절차

To a mixture of 2-chlorothiophene (0.248 mL, 2.68 mmol), tert-butyl piperazine-1-carboxylate (500 mg, 2.68 mmol), and TEA (1.123 mL, 8.05 mmol) in DMF (4 mL) was added Pd(Ph3P)4 (57.8 mg, .05 mmol). The reaction was allowed to heat at 95 °C for overnight. LCMS and TLC showed the starting material peak as well as the triphenyl phosphene ionized M+1 peak. The tryphenyl phosphene showed up at the same retention time as 2-chlorothiophene. No new peak was observed following the reaction so no purification techniques were run. MS (m+1) = not seen

출처 및 근거

ORD 기록
ord-37aa4a46f5494844887cf9e7ccaf1b0d
출처 데이터셋
750 AstraZeneca ELN dataset
원본 링크
출처 보기

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HCID 6228
Dimethylformamide
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