Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanamine, N-methoxy-, hydrochloride (1:1) → 2-(N-Boc)amino-3-(4-cyanophenyl)-N-methoxy-N-methylpropanamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | N-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanine | HCID 7020841 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(N-Boc)amino-3-(4-cyanophenyl)-N-methoxy-N-methylpropanamide | HCID 21070238 | — |
반응 단계
2 g of (N-Boc)-4-cyanophenylalanine, 2.32 g of TBTU, 2.40 ml of DIPEA and 806 mg of N,O-dimethylhydroxylamine hydrochloride are mixed together in 30 ml of DCM. After stirring for 24 hours at RT, the reaction mixture is concentrated to dryness and the residue is then extracted with EtOAc. The organic phase is washed with a pH 2 buffer solution, a saturated NaHCO3 solution and then a saturated NaCl solution. The expected compound crystallizes from a mixture of isopropyl ether and pentane (1.89 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07157454B2 |
| 출처 데이터셋 | uspto-grants-2007_01 |
| ORD ID | ord-90a6d7c751cc4148b1a4a3cdbb4e6014 |
| 출처 메모 | uspto-grants-2007_01 |