HCID 15932586, compound → HCID 54372859, compound

HRID 1588118Notes

Reaction equation

HRID 1588118 reaction equation
[C:1]([NH:4][C@@H:5]1[C@@H:10]([OH:11])[C@H:9]([OH:12])[C@@H:8]([CH2:13][OH:14])[O:7][C@H:6]1[O:15][C@H:16]1[C@@H:31]([OH:32])[C@@H:30]([CH2:33][O:34][C@@H:35]2[O:42][C@H:41]([CH2:43][OH:44])[C@@H:39]([OH:40])[C@H:37]([OH:38])[C@H:36]2[NH:45][C:46](=[O:48])[CH3:47])[O:29][C@@H:18]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][CH3:28])=[O:26])[C@@H:17]1[OH:49])(=[O:3])[CH3:2].C1C(=O)NC(=O)NC=1[C@@H]1O[C@H](COP(OP(O[C@H:73]2[O:78][C@H:77]([CH2:79][OH:80])[C@H:76]([OH:81])[C@H:75]([OH:82])[C@H:74]2[OH:83])(O)=O)(O)=O)[C@@H](O)[C@H]1O>[As](C)(C)(=O)[O-].[Na+].[Cl-].[Mn+2].[Cl-]>[C@@H:18]1([O:12][C@@H:9]2[C@@H:8]([CH2:13][OH:14])[O:7][C@@H:6]([O:15][C@H:16]3[C@@H:31]([OH:32])[C@@H:30]([CH2:33][O:34][C@@H:35]4[O:42][C@H:41]([CH2:43][OH:44])[C@@H:39]([O:40][C@@H:73]5[O:78][C@H:77]([CH2:79][OH:80])[C@H:76]([OH:81])[C@H:75]([OH:82])[C@H:74]5[OH:83])[C@H:37]([OH:38])[C@H:36]4[NH:45][C:46](=[O:48])[CH3:47])[O:29][C@@H:18]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][CH3:28])=[O:26])[C@@H:17]3[OH:49])[C@H:5]([NH:4][C:1](=[O:3])[CH3:2])[C@H:10]2[OH:11])[O:29][C@H:30]([CH2:33][OH:34])[C@H:31]([OH:32])[C@H:16]([OH:15])[C@H:17]1[OH:49]

Participants

5

Reactant 2

HCID 15932586HCID 15932586, compoundHCID 54584734HCID 54584734, compound

Product 1

HCID 54372859HCID 54372859, compound

Reagents, catalysts & solvents 2

HCID 10313134Manganese(2+) dichlorideCatalystHCID 2724247Sodium CacodylateSolvent

Procedure

A solution of compound 19 of Example 19 (85 mg), UDP-galactose, (190 mg), bovine galactosyltransferase (6.25 U) and bovine serum albumin (3 mg) in 30 mM sodium cacodylate buffer (7 mL, pH 7.0) containing manganese chloride (40 umol) was incubated at 37° C. for 22 h. The reaction mixture was diluted to 20 mL and purified as described in Example 21. Yield of the product was 114 mg. The structural identity of titled compound 25 was unambiguously assigned by 1H- and 13C-n.m.r (see Tables 4 and 5, respectively).

Workup

  1. additionThe reaction mixture was diluted to 20 mL
  2. custompurified

Sources & evidence

ORD record
ord-0a5c0b049c9d4a96ad88ce34cc641b1e
Source dataset
uspto-grants-1993_06
Patent number
US05220008

Reaction notes

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