1-Methyl-3-aminopyrazole → HCID 23093057, compound

HRID 2113838Notes

Reaction equation

HRID 2113838 reaction equation
CO[C:3](=[O:12])[C:4]1[CH:9]=[C:8](I)[CH:7]=[C:6]([OH:11])[CH:5]=1.[O:13]([CH2:21][C@H:22](O)[CH3:23])[Si](C(C)(C)C)(C)C.[CH3:25][S:26]([C:29]1[CH:34]=[CH:33][C:32]([SH:35])=[CH:31][CH:30]=1)(=[O:28])=[O:27].[NH2:36][C:37]1[CH:41]=[CH:40][N:39]([CH3:42])[N:38]=1>>[OH:13][CH2:21][CH:22]([CH3:23])[O:11][C:6]1[CH:7]=[C:8]([S:35][C:32]2[CH:33]=[CH:34][C:29]([S:26]([CH3:25])(=[O:28])=[O:27])=[CH:30][CH:31]=2)[CH:9]=[C:4]([CH:5]=1)[C:3]([NH:36][C:37]1[CH:41]=[CH:40][N:39]([CH3:42])[N:38]=1)=[O:12]

Participants

5

Reactant 4

HCID 1372541-Methyl-3-aminopyrazoleHCID 13175135(2R)-1-{[(1,1-Dimethylethyl)(dimethyl)silyl]oxy}propan-2-olHCID 134103233814-25-3HCID 52987947Methyl 3-hydroxy-5-iodobenzoate

Product 1

HCID 23093057HCID 23093057, compound

Procedure

The compound of Production Example 133 was obtained as a colorless amorphous substance using 3-hydroxy-5-iodobenzoic acid methyl ester, (2R)-1-(tert-butyldimethylsiloxy)-2-hydroxypropane, 4-methanesulfonylbenzenethiol and 3-amino-1-methyl-1H-pyrazole, by the same method as in Production Example 74 or 82, a corresponding method, or a combination thereof with an ordinary method.

Workup

  1. customThe compound of Production Example 133 was obtained as a colorless amorphous substance

Sources & evidence

ORD record
ord-093eef70cda84bb185fa98a4e9717a77
Source dataset
uspto-grants-2008_10
Patent number
US07432287B2

Reaction notes

Loading…