참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 9-Fluorenylmethyl chloroformate | HCID 34367 | — |
| 반응물 | Methyl 4-Boc-piperazine-2-acetate | HCID 2756816 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Fmoc-4-Boc-Piperazine-2-acetic acid | HCID 2756796 | 91.7% |
반응 단계
A portion (5.2 g; 20 mmol) of the methyl 4-Boc-piperazine-2-acetate product from the previous step was combined with 60 mL of THF and 60 mL of 1 N NaOH (aqueous) and stirred at room temperature for 6 hours to saponify the methyl ester. The reaction was cooled to 0° C., adjusted to pH 9-10 with 10% HCl(aqueous), and 5.2 g (20 mmol) of FMOC-Cl was added. The reaction was stirred at room temperature for 6 hours, (adding 1 N NaOH (aqueous) to maintain pH 9-10) 1 hour, then acidified with 10% HCl to pH=1. The reaction was extracted twice, the combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 8.56 g of the desired 4-Boc-1-Fmoc-piperazine-2-acetic acid (the compound of formula (XXIV)); 1H NMR (CDCl3) δ 1.4 (s,9), 2.5-3.0 (m,5) 3.9-4.2 (m,6), 4.5 (m,1), 7-25 (t,4), 7.32 (t,4), 7.48 (d,4), 7.75 (d, 4).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06849739B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-1a9145d13d964fe58e1a408fd6fd08e6 |
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| 출처 메모 | uspto-grants-2005_02 |
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