참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Gabapentin | HCID 3446 | — |
| 반응물 | N-Hydroxysuccinimide | HCID 80170 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid | HCID 10977771 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Boc-Asp(OMe) Gabapentin | HCID 131727013 | 98% |
반응 단계
To a solution of Boc-Asp(OMe)-OH (5 g, 20 mmol) in acetonitrile (100 mL) was added N-hydroxysuccinimide (2.53 g, 22 mmol) and N,N-dicyclohexylcarbodiimide (4.5 g, 22 mmol). The reaction was stirred at ambient temperature for 4 h. The reaction mixture was filtered directly into an aqueous solution (100 mL) of gabapentin (3.77 g, 22 mmol) and sodium hydrogencarbonate (1.85 g, 22 mmol) and the resulting mixture stirred at ambient temperature for 16 h. The reaction was concentrated under reduced pressure, the residue dissolved in ethyl acetate/diethyl ether (1:1, 300 mL) and washed with 0.1M aqueous potassium hydrogensulfate (2×500 mL). The organic phase was separated, dried over Na2SO4, filtered, and concentrated to dryness under reduced pressure to afford Boc-Asp(OMe)-Gabapentin as a white solid (7.8 g, 19.5 mmol, 98%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07420002B2 |
|---|
| 출처 데이터셋 | uspto-grants-2008_09 |
|---|
| ORD ID | ord-a5352857d5b9435d9c482e161179277d |
|---|
| 출처 메모 | uspto-grants-2008_09 |
|---|