HCID 19972738, compound → HCID 19972802, compound

HRID 2259903Notes

Reaction equation

HRID 2259903 reaction equation
[ClH:1].[CH2:2]([O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N:11]1[CH2:16][CH2:15][N:14]([CH2:17][C:18]([C:20]2[C:29]3[O:28][C:27]([C:30]4[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=4)=[C:26]([CH3:36])[C:25](=[O:37])[C:24]=3[CH:23]=[CH:22][CH:21]=2)=[O:19])[CH2:13][CH2:12]1)[CH3:3]>CO>[ClH:1].[OH:19][CH:18]([C:20]1[C:29]2[O:28][C:27]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[C:26]([CH3:36])[C:25](=[O:37])[C:24]=2[CH:23]=[CH:22][CH:21]=1)[CH2:17][N:14]1[CH2:15][CH2:16][N:11]([C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][CH2:2][CH3:3])[CH2:12][CH2:13]1

Participants

3

Reactant 1

HCID 19972738HCID 19972738, compound

Product 1

HCID 19972802HCID 19972802, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

This compound was prepared according to Example 17, but starting from the compound prepared in Example 3 rather than that prepared in Example 1. m.p. 241°-242° C. (methanol).

Workup

  1. customThis compound was prepared
  2. customprepared in Example 1

Sources & evidence

ORD record
ord-8ee298b63c014d7abf73d04e960ca76f
Source dataset
uspto-grants-1995_12
Patent number
US05474994

Reaction notes

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