Thiodiglycol → 5-Hydroxy-3-thiapentyl N,N,N',N'-tetrakis(2-chloroethyl)phosphorodiamidate

HRID 417811

반응식

HRID 417811 반응식
[Cl:1][CH2:2][CH2:3][N:4]([CH2:15][CH2:16][Cl:17])[P:5](Cl)([N:7]([CH2:11][CH2:12][Cl:13])[CH2:8][CH2:9][Cl:10])=[O:6].[OH:18][CH2:19][CH2:20][S:21][CH2:22][CH2:23][OH:24].CC(C)([O-])C.[K+]>O1CCCC1.C(OCC)(=O)C>[Cl:17][CH2:16][CH2:15][N:4]([CH2:3][CH2:2][Cl:1])[P:5]([N:7]([CH2:11][CH2:12][Cl:13])[CH2:8][CH2:9][Cl:10])(=[O:6])[O:18][CH2:19][CH2:20][S:21][CH2:22][CH2:23][OH:24]

참가 물질

6

반응 조건

온도
2.5 °C

실험 절차

N,N,N′,N′-Tetrakis(2-chloroethyl)phosphorodiamidoyl chloride, 636 mg (1.745 mmol), and bis(2-hydroxyethyl)sulfide, 1 mL (9.67 mmol), were dissolved in 8 mL anhydrous tetrahydrofuran and cooled to 0-5° C. in an ice-water bath. Potassium tert-butoxide, 1.8 mL of 1 M solution in tetrahydrofuran (1.8 mmol), was added over a 10 minute period, and the reaction mixture kept at 0-5° C. for another 30 minutes. The reaction mixture was allowed to warm to room temperature and stirred at room temperature for 18 hours. It was then diluted with ethyl acetate; and the ethyl acetate layer separated, washed with 1 M hydrochloric acid and brine, then dried over anhydrous magnesium sulfate, and the ethyl acetate removed under vacuum. The crude 5-hydroxy-3-thiapentyl N,N,N′,N′-tetrakis(2-chloroethyl)phosphorodiamidate was purified by column chromatography (silica gel, eluting with 25% ethyl acetate/hexane and 100% ethyl acetate), and obtained as a colorless oil, 335 mg (42.6% yield), identified by HPLC and 1H and 31P NMR.

후처리

  1. temperatureto warm to room temperature
  2. customand the ethyl acetate layer separated
  3. washwashed with 1 M hydrochloric acid and brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe ethyl acetate removed under vacuum
  6. customThe crude 5-hydroxy-3-thiapentyl N,N,N′,N′-tetrakis(2-chloroethyl)phosphorodiamidate was purified by column chromatography (silica gel, eluting with 25% ethyl acetate/hexane and 100% ethyl acetate)
  7. customobtained as a colorless oil, 335 mg (42.6% yield)

출처 및 근거

ORD 기록
ord-029e55fe4fae4964871431f209f3d083
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08093231B2

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