Ammonium → HCID 45110549, compound

HRID 167299Notes

Reaction equation

[BH4-:30].[CH2:36]1[O:37][CH2:38][CH2:39][CH2:40]1.[CH3:34][OH:35].[Cl-:32].[NH4+:33].[Na+:31].[Na:1].[O:2]=[C:3]([CH2:4][C:5]([CH2:6][c:7]1[c:8]([F:15])[cH:9][c:10]([F:14])[c:11]([F:13])[cH:12]1)=[O:16])[N:17]1[CH2:18][c:19]2[n:20]([c:23]([C:26]([F:27])([F:28])[F:29])[n:24][n:25]2)[CH2:21][CH2:22]1>>[O:2]=[C:3]([CH2:4][CH:5]([CH2:6][c:7]1[c:8]([F:15])[cH:9][c:10]([F:14])[c:11]([F:13])[cH:12]1)[OH:16])[N:17]1[CH2:18][c:19]2[n:20]([c:23]([C:26]([F:27])([F:28])[F:29])[n:24][n:25]2)[CH2:21][CH2:22]1

Participants

Reactant 8

HCID 8028Tetrahydrofuran

HCID 28123Borohydride

HCID 5360545Sodium

HCID 98875881-(3-(trifluoromethyl)-5,6-dihydro(1,2,4)triazolo(4,3-a)pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl)butane-1,3-dione

Product 1

HCID 45110549HCID 45110549, compound

Sources & evidence

ORD record: ord-b0c223e4764143e0a03e5a6b29af3ccd
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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