4-Methyl-2-phenoxymethyl-6,7-dihydro-pyrazolo[1,5-a]pyrazine → 2-Phenoxymethyl-6,7-dihydro-pyrazolo[1,5-a]pyrazine
Reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][N:10]1[C:14]([CH:15]=O)=[CH:13][C:12]([CH2:17][O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[N:11]1)(C)(C)C.CC1C2N(N=C(COC3C=CC=CC=3)C=2)CCN=1>>[O:18]([CH2:17][C:12]1[CH:13]=[C:14]2[CH:15]=[N:7][CH2:8][CH2:9][N:10]2[N:11]=1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1Participants
3
Procedure
The compound was prepared from [2-(5-formyl-3-phenoxymethyl-pyrazol-1-yl)-ethyl]-carbamic acid tert-butyl ester using the method described in the preceding example 24 (4-methyl-2-phenoxymethyl-6,7-dihydro-pyrazolo[1,5-a]pyrazine).
Sources & evidence
- ORD record
- ord-f7c82826ffaa4693a8c877669f28dbce
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08703946B2
Reaction notes
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