홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Triethylamine → HCID 20638914, 화합물

HRID 565406
노트
인쇄 미리보기

반응식

HRID 565406 반응식
O[C:2]([CH2:4][CH2:5][CH2:6][CH2:7][C@H:8]1[C@@H:16]2[C@@H:11]([NH:12][C:13]([NH:15]2)=[O:14])[CH2:10][S:9]1)=[O:3].Cl.[CH3:18][O:19][C:20](=[O:28])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][NH:26][CH3:27].C(N(CC)CC)C.P(=O)([O-])[O-].P(=O)([O-])[O-].P(=O)([O-])[O-].P(=O)([O-])[O-].P(=O)([O-])[O-].P(=O)([O-])[O-].N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1.N1C2C=CC=C(O[P+](N(C)C)(N(C)C)N(C)C)C=2N=N1>CN(C)C=O>[CH3:27][N:26]([CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][C:20]([O:19][CH3:18])=[O:28])[C:2](=[O:3])[CH2:4][CH2:5][CH2:6][CH2:7][C@H:8]1[C@@H:16]2[C@@H:11]([NH:12][C:13]([NH:15]2)=[O:14])[CH2:10][S:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 171548BiotinHCID 21932558Methyl 6-(methylamino)hexanoate--hydrogen chloride (1/1)HCID 178486077HCID 178486077, 화합물2회

생성물 1

HCID 20638914HCID 20638914, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a 500 mL round bottom flask, charged with 9.00 g (36.8 mmol) of biotin (Sigma Chemical Company), 7.93 g (40.5 mmol, 1.1 equiv.) of amine hydrochloride 12, and 200 mL of anhydrous dimethylformamide was added 17 mL of triethylamine (120 mmol) followed by 17.1 g (38.7 mmol, 1.05 equiv.) of benzotriazolyloxytris(dimethylamino)phosphonium hexaphosphonate (BOP, commercially available from Aldrich Chemical Company and Chem-Impex International, Wood Dale, Ill.) coupling agent. The reaction was stirred at room temperature for 13 h and then concentrated. The residue was diluted with 100 mL of 2-propanol and 300 mL of methylene chloride and the resulting mixture was washed with 2×150 mL aliquots of 1N aqueous HCl and then with 150 mL of de-ionized water. The organic phase was dried with anhydrous magnesium sulfate and vacuum filtered. The solids were rinsed with 100 mL of 25% 2-propanol/methylene chloride. The combined filtrates were concentrated. The residue was chromatographed on 9×22 cm of silica gel, eluting with 20% methanol/ethyl acetate. The fractions containing product (13) were combined and concentrated via rotary evaporation. The residue was chromatographed on 7×18 cm of RP-18 silica gel, eluting with 800 mL of 50:50 methanol/water, 1 liter of 55:45 methanol/water and 2 liters of 60:40 methanol/water. The fractions containing product (13) were combined and concentrated, first via rotary evaporation and finally under full vacuum pump pressure (<0.5 mm Hg) to afford 11.58 of the product (13) as a near colorless oil: 1H NMR (d6-DMSO) d 6.42 (1H, s), 6.33 (1H, s), 4.29 (1H, m), 4.12 (1H, m), 3.57 (3H, s), 3.22 (2H, t), 3.09 (1H, m), 2.91 and 2.77 (3H, 2 s), 2.81 (1H, dd), 2.57 (1H, d), 2.34-2.19 (4H, m) and 1.70-1.10 (12H, m) ppm; 1H NMR (CD3pk OD) d 4.48 (1H, dd), 4.29 (1H, dd), 3.63 and 3.62 (3H, 2 s), 3.34 (2H, t), 3.20 (1H, m), 3.02 and 2.88 (3H, 2 s), 2.91 (1H, dd), 2.68 (1H, d), 2.43-2.27 (4H, m) and 1.80-1.20 (12H, m) ppm; Thin Layer Chromatography (Visualization with p-aminocinnimaldehyde spray); Silica Gel, Rf=0.31 ({fraction (80/20)} ethyl acetate/methanol); RP-18 Silica Gel, Rf=0.29 ({fraction (60/40)} methanol/water).

후처리

  1. concentrationconcentrated
  2. additionThe residue was diluted with 100 mL of 2-propanol and 300 mL of methylene chloride
  3. washthe resulting mixture was washed with 2×150 mL aliquots of 1N aqueous HCl
  4. dry with materialThe organic phase was dried with anhydrous magnesium sulfate and vacuum
  5. filtrationfiltered
  6. washThe solids were rinsed with 100 mL of 25% 2-propanol/methylene chloride
  7. concentrationThe combined filtrates were concentrated
  8. customThe residue was chromatographed on 9×22 cm of silica gel
  9. washeluting with 20% methanol/ethyl acetate
  10. additionThe fractions containing product (13)
  11. concentrationconcentrated via rotary evaporation
  12. customThe residue was chromatographed on 7×18 cm of RP-18 silica gel
  13. washeluting with 800 mL of 50:50 methanol/water, 1 liter of 55:45 methanol/water and 2 liters of 60:40 methanol/water
  14. additionThe fractions containing product (13)
  15. concentrationconcentrated, first via rotary evaporation and finally under full vacuum pump pressure (<0.5 mm Hg)

출처 및 근거

ORD 기록
ord-d395050729c149de81d3c329c18a3ae1
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06172045B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트