HCID 4594296, compound → HCID 58034759, compound

HRID 1914831Notes

Reaction equation

HRID 1914831 reaction equation
NC1N2N=C(C)C=C2N=CC=1C=O.[NH2:14][C:15]1[N:20]2[N:21]=[C:22]([N:24]3[CH2:29][CH2:28][O:27][CH2:26][CH2:25]3)[N:23]=[C:19]2[N:18]=[CH:17][C:16]=1[C:30](OCC)=[O:31]>>[NH2:14][C:15]1[N:20]2[N:21]=[C:22]([N:24]3[CH2:25][CH2:26][O:27][CH2:28][CH2:29]3)[N:23]=[C:19]2[N:18]=[CH:17][C:16]=1[CH:30]=[O:31]

Participants

3

Reactant 2

HCID 4594296HCID 4594296, compoundHCID 58034374HCID 58034374, compound

Product 1

HCID 58034759HCID 58034759, compound

Procedure

Compound (12-2) was synthesized in a similar manner to the procedure for example (1-1) and (1-2), but using ethyl 7-amino-2-(morpholin-4-yl)[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate (12-1) as a starting material.

Sources & evidence

ORD record
ord-0875d10b17244b0797d542545bc664bf
Source dataset
uspto-grants-2013_12
Patent number
US08614221B2

Reaction notes

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