Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester → (2S)-2-(azepane-1-carbonylamino)-4-methylpentanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester | HCID 10593708 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2S)-2-(azepane-1-carbonylamino)-4-methylpentanoic acid | HCID 7530182 | 93.5% |
반응 단계
A solution of (S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid benzyl ester (38.5 g, 111 mmol) in 600 mL of THF was hydrogenated at 50 psi over 20% Pd/C (2.00 g) for 17 minutes. The reaction mixture was filtered through celite and concentrated to dryness. The residue was heated in 50 mL of hexane. The resulting suspension was cooled, and the solid was collected by filtration and washed with hexane. The solid was dried at room temperature under vacuum to give (S)-2-[(azepane-1-carbonyl)-amino]-4-methyl-pentanoic acid as a white solid (26.6 g, 93%); mp 88-89° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06316440B1 |
| 출처 데이터셋 | uspto-grants-2001_11 |
| ORD ID | ord-7b382acd046c4ea3bccd4708b2803601 |
| 출처 메모 | uspto-grants-2001_11 |