HCID 607618, compound → HCID 10138215, compound

HRID 352333Notes

Reaction equation

HRID 352333 reaction equation
[OH:1][CH:2]1[C@@H:6]([NH:7][C:8]([C@@H:10]([NH:15]C(C2C=CC3SC4C(=CC=CC=4)NC=3C=2)=O)[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:9])[CH2:5][CH2:4][O:3]1.[C:32]1([C:46]([OH:48])=O)[C:45]2[NH:44][C:43]3[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=3)[S:37][C:36]=2[CH:35]=[CH:34][CH:33]=1>>[OH:1][CH:2]1[C@@H:6]([NH:7][C:8]([C@@H:10]([NH:15][C:46]([C:32]2[C:45]3[NH:44][C:43]4[C:38](=[CH:39][CH:40]=[CH:41][CH:42]=4)[S:37][C:36]=3[CH:35]=[CH:34][CH:33]=2)=[O:48])[CH2:11][CH:12]([CH3:13])[CH3:14])=[O:9])[CH2:5][CH2:4][O:3]1

Participants

3

Reactant 2

HCID 607618HCID 607618, compoundHCID 10181824HCID 10181824, compound

Product 1

HCID 10138215HCID 10138215, compound

Procedure

The experimental protocol used is identical to that described for compound 17, with 10H-phenothiazine-1-carboxylic acid replacing 10H-phenothiazine-2-carboxylic acid. Yellow powder. Melting point: 99-101 ° C.

Sources & evidence

ORD record
ord-414938599f4245b1863dcc683139e944
Source dataset
uspto-grants-2004_06
Patent number
US06747024B1

Reaction notes

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