Acetonitrile → Allyl [(4-amino-5-benzyl-2-pyrimidinyl)sulfanyl]acetate
반응식
[NH2:1][C:2]1[C:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][N:5]=[C:4]([S:15][CH2:16][C:17]([OH:19])=[O:18])[N:3]=1.[CH:20]1(N=C=NC2CCCCC2)[CH2:25]CCC[CH2:21]1.C(O)C=C.CC#N>CN(C=O)C.CN(C)C1C=CN=CC=1.C(O)(C(F)(F)F)=O>[CH2:25]([O:18][C:17](=[O:19])[CH2:16][S:15][C:4]1[N:3]=[C:2]([NH2:1])[C:7]([CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][N:5]=1)[CH:20]=[CH2:21]참가 물질
8
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
(4-Amino-5-benzyl-pyrimidin-2-ylsulfanyl)-acetic acid (0.25 mmol, 69 mg), dicyclohexylcarbodiimide (0.3 mmol, 62 mg) and allyl alcohol (0.3 mmol, 18 mg) were dissolved in 1 ml of DMF, and a catalytic amount of 4-dimethylaminopyridine (approx. 1–3 mg) was added. After shaking the mixture for 24 h at r.t., the title compound, MS: m/e=316.2 (M+H+), was obtained from the reaction mixture by HPLC chromatography (YMC CombiPrep C18 column 50×20 mm, solvent gradient 10–95% CH3CN in 0.1% TFA(aq) over 6.0 min, λ=230 nm, flow rate 40 ml/min).
출처 및 근거
- ORD 기록
- ord-74da07a0b0e14852b581171b1b739882
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07138404B2
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