Hydrochloric Acid → HCID 68706552, compound

HRID 1526095Notes

Reaction equation

HRID 1526095 reaction equation
[Cl-:1].[Ca+2].[Cl-].[BH4-].[Na+].C[O:7][C:8](=O)[C:9]1[CH:14]=[CH:13][N:12]=[C:11]([N:15]2[C:19](=[O:20])[C:18]([C:21]3[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=3)=[CH:17][NH:16]2)[CH:10]=1.Cl>C(O)C>[ClH:1].[OH:7][CH2:8][C:9]1[CH:14]=[CH:13][N:12]=[C:11]([N:15]2[C:19](=[O:20])[C:18]([C:21]3[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=3)=[CH:17][NH:16]2)[CH:10]=1

Participants

6

Procedure

197 mg (1.77 mmol) calcium chloride and 319 mg (8.44 mmol) sodium borohydride are initially introduced into 26 ml ethanol, 50 mg (169 μmol) of the compound from Example 42 are added in portions at 0° C. and the mixture is stirred overnight at RT. The reaction mixture is adjusted to a slightly acid pH by addition of 1 M hydrochloric acid and concentrated and the residue is purified by means of preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient with addition of 0.1% conc. hydrochloric acid).

Workup

  1. additionare added in portions at 0° C.
  2. concentrationconcentrated
  3. customthe residue is purified by means of preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient with addition of 0.1% conc. hydrochloric acid)

Sources & evidence

ORD record
ord-126e4e552a4544db87bd48f448e49f94
Source dataset
uspto-grants-2015_07
Patent number
US09085572B2

Reaction notes

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