Monobasic potassium phosphate → Ribavirin

반응식

[NH:1]1C=CN=N1.[C@@H:6]1([N:15]2C3N=C[N:21]=[C:19]([OH:20])[C:18]=3[N:17]=[CH:16]2)[O:14][C@H:11]([CH2:12][OH:13])[C@@H:9]([OH:10])[C@H:7]1[OH:8].P([O-])(O)(O)=O.[K+]>>[CH:16]1[N:15]([C@@H:6]2[O:14][C@H:11]([CH2:12][OH:13])[C@@H:9]([OH:10])[C@H:7]2[OH:8])[N:1]=[C:18]([C:19]([NH2:21])=[O:20])[N:17]=1

참가 물질

반응물 3

HCID 516951Monobasic potassium phosphate

HCID 178418936HCID 178418936, 화합물

HCID 178521066(2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-hydroxypurin-9-yl)oxolane-3,4-diol

생성물 1

HCID 37542Ribavirin

실험 절차

By using a substrate solution (pH 6.0) containing 40 mM triazole as the base donor, 60 mM inosine as the saccharide residue donor and 40 mM potassium dihydrogenphosphate, reactions were carried out in the same manner as in Example 1 at respective reaction temperature (40° to 70° C.) for 24 hours to produce ribavirin. The results are shown in Table 8.

출처 및 근거

ORD 기록: ord-ad34d5e319f442798901411e2fa06cde
출처 데이터셋: uspto-grants-1993_11
DOI: 10.6084/m9.figshare.5104873.v1
특허 번호: US05258301

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