1H-Pyrazolo[4,3-c]pyridine → HCID 71009368, compound

HRID 1527310Notes

Reaction equation

HRID 1527310 reaction equation
[NH:1]1[C:9]2C=CN=CC=2C=N1.[C:10]([C:13]1[C:21]2[C:16](=[CH:17]N=C(C)[CH:20]=2)[N:15]([CH2:23][C:24]([OH:26])=[O:25])[N:14]=1)(=[O:12])[NH2:11]>>[C:10]([C:13]1[C:21]2[CH:20]=[N:1][CH:9]=[CH:17][C:16]=2[N:15]([CH2:23][C:24]([OH:26])=[O:25])[N:14]=1)(=[O:12])[NH2:11]

Participants

3

Reactant 2

HCID 199305001H-Pyrazolo[4,3-c]pyridineHCID 68283471HCID 68283471, compound

Product 1

HCID 71009368HCID 71009368, compound

Procedure

was prepared from 1H-pyrazolo[4,3-c]pyridine [271-52-3] by using the same procedures as for the preparation of (3-carbamoyl-5-methyl-pyrazolo[3,4-c]pyridin-1-yl)-acetic acid (Scheme A27). MS (LC-MS): 221 [M+H]+, tR (HPLC conditions k): 0.19 min.

Workup

  1. custom0.19 min.

Sources & evidence

ORD record
ord-650c79a47fa14855b3fb7c18a731e7fa
Source dataset
uspto-grants-2015_07
Patent number
US09085555B2

Reaction notes

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