Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458925생성일: 2026년 10월 25일
O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate → 2-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}ethane-1-sulfonic acid
https://huagongshe.com/reaction/458925
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | Tetrabutylammonium taurine | HCID 21896665 | — |
| 반응물 | N-Boc-p-hydroxyphenylglycine | HCID 21896684 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}ethane-1-sulfonic acid | HCID 71363085 | — |
반응 단계
N-Boc-4-hydroxyphenylglycine (1.00 g, 3.21 mmol) was dissolved in DMF (5 ml) and tetrabutylammonium taurine (2.36 g, 6.42 mmol) was added together with additionally 5 ml DMF. The resulting suspension was cooled on ice and TBTU (1.24 g, 3.85 mmol) was added. The ice bath was removed after 30 min and the mixture was stirred for 2 hours before it was filtered and concentrated. TFA in DCM (20%, 20 ml) was added and the reaction mixture was stirred overnight. Ethanol (20 ml) was added and the solvents evaporated. The crude product was refluxed in ethanol (100 ml) for 1 hour. Filtration yielded the pure title compound as a white solid, 626 mg (71%). NMR (DMSO-d6) 2.4–2.6 (m, 2H), 3.2–3.4 (m, 2H), 4.79 (s, 1H), 6.78 (d, 2H), 7.23 (d, 2H), 8.22 (t, 1H), 8.4 (brs, 3H), 9.7 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07192945B2 |
|---|
| 출처 데이터셋 | uspto-grants-2007_03 |
|---|
| ORD ID | ord-ac06406818464c079478a84f31c3f559 |
|---|
| 출처 메모 | uspto-grants-2007_03 |
|---|