Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
L-Lysine → 5-(4-Benzyloxycarbonylaminobutyl)-3-methyl-2-thiohydantoin
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | L-Lysine | HCID 5962 | — |
| 반응물 | Methyl isothiocyanate | HCID 11167 | — |
| 반응물 | methyl (2S)-2-amino-6-(phenylmethoxycarbonylamino)hexanoate | HCID 6994982 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-(4-Benzyloxycarbonylaminobutyl)-3-methyl-2-thiohydantoin | HCID 21507682 | 22.4% |
반응 단계
A solution of Nε-benzyloxycarbonyl-L-lysine methyl ester (4.66 g., 0.016 mol.) (prepared from L-lysine according to the method of Bergmann et al., J. Biol. Chem. 1935, 111, 245) in acetonitrile (20 ml.) was treated with methyl isothiocyanate (1.16 g., 0.016 mol.) and the mixture heated at reflux for 3 hours. The solvent was removed in vacuo and the residual oil triturated with ethanol to give a white solid which recrystallised from ethanol to give the title compound as colourless needles (1.2 g.) m.p. 135°C. (Found: C, 57.3; H, 6.4; N, 12.2; C16H21N3O3S requires: C, 57.3; H, 6.3; N, 12.5%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US03984430 |
| 출처 데이터셋 | uspto-grants-1976_10 |
| ORD ID | ord-ac5d9645333b464685fd8da40dd721f4 |
| 출처 메모 | uspto-grants-1976_10 |