Thionyl Chloride → HCID 69701695, compound

HRID 1266044Notes

Reaction equation

HRID 1266044 reaction equation
O[CH:2]([C:7]1[CH:12]=[CH:11][C:10]([C:13]2[N:18]3[CH2:19][CH2:20][C:21]4[NH:22][C:23](=[O:26])[CH:24]=[CH:25][C:16]([C:17]=43)=[CH:15][N:14]=2)=[CH:9][CH:8]=1)[CH2:3][CH:4]([CH3:6])[CH3:5].S(Cl)([Cl:29])=O>>[Cl:29][CH:2]([C:7]1[CH:12]=[CH:11][C:10]([C:13]2[N:18]3[CH2:19][CH2:20][C:21]4[NH:22][C:23](=[O:26])[CH:24]=[CH:25][C:16]([C:17]=43)=[CH:15][N:14]=2)=[CH:9][CH:8]=1)[CH2:3][CH:4]([CH3:6])[CH3:5]

Participants

3

Procedure

This compound was prepared from intermediate 228 and thionyl chloride according to the procedure used in Example 171. Received 8.36 g (91%)

Sources & evidence

ORD record
ord-e24001d3ac3e4446a19b99c201c6a44e
Source dataset
uspto-grants-2003_04
Patent number
US06548494B1

Reaction notes

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